Merck

To make a difference in the lives of people globally through our innovative medicines, vaccines, and animal health products. We are committed to being the premier, research-intensive biopharmaceutical company and are dedicated to providing leading innovations and solutions for today and the future.

Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. The Analytical Research & Development department of Merck Research Laboratories is seeking applicants for an Associate Principal Scientist position available at its Rahway, New Jersey research facility. The Associate Principal Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of chemistry, engineering, and lab informatics disciplines to enable development of active pharmaceutical ingredients (APIs). The successful candidate must function well and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. Research experience should demonstrate successful application and management of team members in state-of-the-art analytical techniques to solve chemistry problems, including chiral / achiral separations (HPLC / SFC/ GC / CE / IC), spectroscopic techniques (NMR, MS, UV-VIS / IR / Fluorescence / Raman), solid-state analysis (X-ray diffraction, DVS, DSC, TGA and microscopy), and classical wet chemistry techniques. Additional experience in synthetic / physical organic chemistry, mechanistic / kinetic studies of chemical reactions, continuous monitoring using process analytical tools, or lab automation / informatics is considered a plus. Applicants must have effective organizational, multi-tasking, oral / written communications skills, show scientific leadership, and a desire to conduct research and publish. In addition, experience leading small groups of technical personnel and analytical projects will aid in distinguishing candidates. Education: + Ph.D with at least 4 years’ experience OR M.S. with at least 8 years of experience in the pharmaceutical industry within chemistry or analytical chemistry, or a related field. Required: + Excellent verbal and written communication skills, demonstrated creativity, strong interpersonal skills + Ability to work in a team environment with cross-functional interactions is essential + Minimum of 4 years of experience in the Pharmaceutical Industry within chemistry, analytical chemistry or related field Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Chemistry_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Associate Principal Scientist_ **Primary Location:** NA-US-NJ-Rahway **Requisition ID:** _CHE005790_
Merck Rahway, NJ
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. The Cardiovascular Disease therapeutic area at Merck is seeking an in vivo Scientist who has hands on experience with rodent models of cardiovascular disease or pulmonary hypertension. The individual will be expected to contribute to the execution, data analysis and record keeping of in vivo studie, including the operation of sensitive and highly complex laboratory equipment. Other desirable attributes include strong self-motivation, solid written and oral communication skills, and being able to work productively in a collaborative and cross functional team environment. Education: + Bachelor of Science with 3 years industry experience or MS degree Required: + A minimum of 2 years of experience with rodent handling, tissue collection, blood collection. + Ability to perform calculations to complete research test results, collate large data sets, perform statistical analysis of lab results (Excel, Prism, etc.) and maintain notes. + Must be willing to learn and work as a team member in an environment where attention to detail and a sense of urgency are critical Preferred: + Jugular vein venipuncture, animal model development, rodent surgical skills Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Biology-Discovery_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Scientist, In Vivo – Cardiovascular Diseases_ **Primary Location:** NA-US-MA-Boston **Requisition ID:** _BIO005044_
Merck Boston, MA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. As part of the Merck Manufacturing Division, and operating within Global Vaccines and Biologics Commercialization (GVBC), the Biologics Process Development and Commercialization (BPDC) department provides manufacturing sciences expertise, through technical process leadership and laboratory capabilities, in the commercialization and post-launch support of Merck’s biologics pipeline. Working closely with colleagues across the biologics network, including Merck Research Labs (MRL), Operations, and Global Technical Operations (GTO), our department supports upstream cell culture, downstream purification, analytical testing and characterization, and technology transfer of biological processes (therapeutic proteins) from Phase III through commercial launch and transfer to the commercial supply network. For the in-line support of commercial biologics, including, but not limited to, KEYTRUDA and ZINPLAVA, we provide deep scientific support for investigations, post-launch process enhancements, technology transfers, and the development and characterization of next generation processes post-approval. For pipeline biologics, we support various commercialization activities, including scale-up/scale-down, process characterization and validation, technology transfer and authoring of regulatory submissions. Under the general scientific and administrative direction of the Kenilworth lead of BPDC Process Analytics, and working in conjunction with internal and external partners, this individual will support in-process analytical and characterization testing of late stage drug substance process development and characterization, technology transfer, post-approval process development and validation studies for Merck’s commercial biologics products as well as pipeline programs. The individual will demonstrate strong scientific, experimental and technology transfer leadership and skills focused on common analytical methods used for biologics. Technical Scope: + Primary focus will be on in-process analytics, but with a working knowledge of the various aspects of product manufacture and functional area interdependencies, including cell culture, purification, and site readiness. + Represents functional area on cross-functional and cross-divisional teams. + Leads process and product comparability assessments to support facility and process changes during late stage development or in-line product support. + Leads matrix teams responsible for in-process characterization testing of laboratory-scale and manufacturing-scale studies to support commercial process validation, characterization, and investigation evaluations, including studies performed either in-house or externally. + Provides technical leadership for method development and qualification, as well as the execution of (internal) or management of (external) laboratory activities. + Authors required regulatory and technical documentation according to standard Merck practices. + Shows flexibility and agility in responding to changing needs across BPDC and Merck. Education: + Bachelors Degree or higher in Analytical Sciences, Biological Sciences, Chemical Engineering, Biological Engineering, or related field with a minimum of ten (10) years (for BS), a minimum of eight (8) years (for MS), or a minimum of four (4) years (for PhD) of relevant industry experience. Required: + In-depth technical knowledge and expertise in the characterization of biological molecules. + Experience with HPLC and/or UPLC method development and qualification. + Experience with people management and/or team leadership in late-stage development or commercialization teams. Preferred: + Working knowledge of statistical methods for DOE design and data analysis (e.g., JMP or Design Expert software), statistical process control (SPC), multivariate analysis (MVA), and/or process analytical technologies (PAT) techniques for biologics processes + Working understanding of US/EU regulatory requirements (e.g. comparability, method transfer). + Working knowledge of cGMPs. + Working knowledge of mass spectrometry. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Process Engineering_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Associate Principal Scientist, Process Analytics - Biologics Process Development and Commercialization_ **Primary Location:** NA-US-NJ-Kenilworth **Requisition ID:** _PRO016768_
Merck Kenilworth, NJ
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its 125-year legacy. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. The Learning Specialist supports and facilitates learning and development activities for a defined client base within an operation or function. The role supports Learning Leads and Sr. Learning Specialists in the execution of the L&D strategy through consulting and delivery on appropriate learning solutions. S/he interacts with and influences (first line) to mid-level managers to understand business goals and performance needs, participates in the development of plans and executes learning plans aligned to the business strategy. Success in this role depends on the candidate’s ability to collaborate with leaders in the business, Learning Leads, and other Learning Specialists, as well as work cross-functionally to act as a partner and point of contact for the business’ performance needs and communicate them to support design and delivery of learning solutions. Responsibilities: Reporting to the Learning Lead, the primary focus of the Learning Specialist is to: + Diagnose a client’s learning challenges and propose solutions + Design and develop necessary learning solutions to drive positive business results + Partner with Subject Matter Experts (SME) to develop training content + Leverage and strengthen the skills of SMEs to ensure effective training solutions and sustained results + Lead or be a member of a high performing team assigned to develop standard process for the organization + Effectively use metrics and measurement to ensure that learning solutions result in desired on-the-job behavior changes + Maintain compliant training curriculums and job codes in the area they support + Deliver Training if needed + Applies team effectiveness skills, listening and integrating diverse perspectives from across the work group; contributes and adds value to the achievement of team goals. Education: + Bachelor’s Degree or higher in Science, Engineering or another technical discipline Required: + Minimum two years’ experience in a highly regulated industry (preferably biotech/pharmaceutical manufacturing) + Proven interpersonal skills, as well as very strong verbal and written communication skills + Design and Development of Training Programs + Facilitation and Presentation skills Preferred: + Project management experience + Collaborative and a team player, able to develop rapport and credibility with key stakeholders + Demonstrates a sense of urgency, when applicable, to drive sustained business results Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need an accommodation for the application process please email us at staffingaadar@merck.com . Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Technical Training_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Learning Specialist_ **Primary Location:** NA-US-PA-West Point **Requisition ID:** _TEC001233_
Merck West Point, PA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. **This is a Night shift position, Monday - Friday.** Responsible for providing reliability maintenance engineering support to ensure optimum performance in equipment, systems, documentation and asset utilization in the Plant Maintenance Department. Is also responsible for other maintenance planning and administrative functions. Maintains equipment data, PM and calibration plans and coordinates the calibration program within the business unit. Develops equipment specific training outlines and develops and tracks metrics. Primary activities include, but are not limited to: + Project Management (50%) + Responsible for all aspects of project management (analysis, design, planning, scheduling, securing funds, coordinating equipment, procurement, cost control, supervising, contracted resources, status reporting, communication, ensuring team involvement) + Develop spare parts lists for new equipment + Participates in Factory Acceptance Testing (FAT) for new and modified equipment installations + Responsible for all aspects of process change control (evaluation, approval, communication, planning scheduling, validation and project documentation, auditing, training, implementation) + Design/conduct scientific experiments to support process change proposals and product development for in line and new products; identifying and understanding science of in line processes and transferring that knowledge to appropriate personnel + Initiate and manage WCRs + Write and execute qualifications + Problem Resolution/Troubleshooting: (15%) + Responsible for identifying and applying creative/technical solutions aimed at cost reduction, improved yields and quality of products and/or facilities which meet all regulatory requirements + Apply technical skills and ingenuity to correct equipment problems that result in production downtime or consume excessive maintenance resources + Effectively transfer into production of new technologies + Consult with departmental resources including Coaches and mechanics to support real-time processing decisions and support areas in determining technical and strategic directions and initiatives for the plant + MOE improvements, investigations and follow-ups to improve line quality, output and/or total production costs; + Assist with atypical investigations + Development & Maintenance of Records, Standards, PMs and Calibrations (25%) + Responsible for PM and calibration program development, changes and optimization to include Task List for PM's and calibrations, linked CI & CR, equipment classification characteristics for internal SAP calibrations, Maintenance Items; Initiate & process maintenance change control for equipment, PM and calibration program + Responsible for spare part data additions, changes and deletions BOM's (equipment, FLOC), Task List (required components) + Maintain and analyze equipment data & historical records to help anticipate maintenance needs and trends Analyzes equipment & maintenance performance, perform RCM and RCFA + Work with Maintenance Planner/and/or Mechanic to develop calibration standards and perform Critical Calibration Out of Tolerance Reporting + Administrative (10%) + Assure all equipment manuals are updated and adequate + Update/ print other documentation; assist in designing & monitoring an effective and economical PM/PdM system driven towards Reliability Centered Maintenance (RCM) + Perform specific maintenance related SOP changes + Link spare parts to equipment, creates modified or new parts drawing and keeps Bill of Materials current + Make changes to setup sheets (for packaging lines) resulting from tactical projects. Education: + High School Diploma with a minimum of ten (10) years of Maintenance experience + Associate Degree in a technical field with a minimum of seven (7) years of Maintenance experience + Bachelor Degree or higher in a science discipline with a minimum of three (3) years of Maintenance experience (preferred) Required: + Strong technical problem-solving abilities + Ability to manage investigations/projects to a schedule + In-depth knowledge of computerized maintenance management system (i.e., SAP), maintenance work management process, production related standards and project management + Knowledge of production and packaging related equipment, preventive maintenance and calibration control systems, in depth understanding of plant wide flow, and facilities and construction techniques and processes. + Knowledge of most utility operations and production processes + Proficient in Word and Excel. Preferred: + Experience in Deviation Management investigation process, authoring in-depth investigations and applying sound Root Cause Analysis principles + Previous involvement in regulatory inspection activities Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Engineering Generic_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Reliability Engineer (Night Shift)_ **Primary Location:** NA-US-NC-Wilson **Requisition ID:** _ENG003692_
Merck Wilson, NC
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-CT-Hartford_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (New England)_ **_Primary Location:_** _NA-US-MA-Boston_ **_Requisition ID:_** _MED003358_
Merck Hartford, CT
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-NJ-Jersey City, NA-US-NY-Long Island_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (New York Metro)_ **_Primary Location:_** _NA-US-NY-New York City_ **_Requisition ID:_** _MED003347_
Merck Jersey City, NJ
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-Nebraska, NA-US-AZ-Phoenix, NA-US-New Mexico, NA-US-KS-Kansas City, NA-US-Utah, NA-US-Wyoming_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (Plain States)_ **_Primary Location:_** _NA-US-CO-Denver_ **_Requisition ID:_** _MED003354_
Merck Phoenix, AZ
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-NJ-Jersey City, NA-US-NY-Long Island_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (New York Metro)_ **_Primary Location:_** _NA-US-NY-New York City_ **_Requisition ID:_** _MED003347_
Merck Long Island, NY
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-Nebraska, NA-US-AZ-Phoenix, NA-US-New Mexico, NA-US-KS-Kansas City, NA-US-Utah, NA-US-Wyoming_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (Plain States)_ **_Primary Location:_** _NA-US-CO-Denver_ **_Requisition ID:_** _MED003354_
Merck Kansas City, KS
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-NJ-Jersey City, NA-US-NY-Long Island_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (New York Metro)_ **_Primary Location:_** _NA-US-NY-New York City_ **_Requisition ID:_** _MED003347_
Merck New York City, NY
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf HJ042018 Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-Nevada, NA-US-Hawaii, NA-US-CA-Sacramento_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (Northern CA, NV, HI)_ **_Primary Location:_** _NA-US-CA-San Francisco_ **_Requisition ID:_** _MED003351_
Merck San Francisco, CA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-Nebraska, NA-US-AZ-Phoenix, NA-US-New Mexico, NA-US-KS-Kansas City, NA-US-Utah, NA-US-Wyoming_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (Plain States)_ **_Primary Location:_** _NA-US-CO-Denver_ **_Requisition ID:_** _MED003354_
Merck Denver, CO
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-CT-Hartford_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (New England)_ **_Primary Location:_** _NA-US-MA-Boston_ **_Requisition ID:_** _MED003358_
Merck Boston, MA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At Merck, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. The MSL is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional claims about any drug, vaccine or biologic product. MSLs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to Merck. MSLs also respond to scientific questions from SLs, including questions about Merck products. MSLs have no sales objectives or accountability for prescribing or sales of any Merck product and are required to avoid any situations that could create the appearance that they have such responsibilities. An MSL may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient. Primary Activities: + Develop professional relationships and communicate with national and regional scientific leaders to ensure access to medical and scientific information on areas of therapeutic interest and Merck products. + Conduct peer to peer scientific discussions and maintain a reliable presence with those scientific leaders to ensure they have a medical contact within Merck. + Review headquarters-directed education and training to maintain current knowledge and understanding of dynamic scientific and clinical environment in Merck’s areas of interest. + Direct scientific leader inquiries on issues outside of MSL scope of responsibilities (e.g., research, grants) to appropriate Merck resources consistent with applicable policies. + When requested by MRL, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs + In response to unsolicited requests from scientific leaders, provide areas of interest and general high-level information regarding the Merck Investigator Study Program process. + Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner. Education: + MD, PharmD, or PhD Required: + A minimum of 3 years of clinical (patient care) or deep research experience in Oncology beyond that obtained in the terminal degree program. + Capable of conducting doctoral level discussions with key customers + Strong focus on scientific education and dialogue + Business and market knowledge, including quality management. + Excellent interpersonal, communication, and networking skills + Must possess a thorough understanding of FDA, OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Must be able to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access). .Preferred: + Field-based medical experience + Clinical research experience + Demonstrated record of scientific/medical publication Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf HJ042018 Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Medical Affairs Generic Field Based ONC_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _NA-US-Nevada, NA-US-Hawaii, NA-US-CA-Sacramento_ **_Title:_** _Oncology Medical Science Liaison - Solid Tumors (Northern CA, NV, HI)_ **_Primary Location:_** _NA-US-CA-San Francisco_ **_Requisition ID:_** _MED003351_
Merck Sacramento, CA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. Merck is currently seeking a qualified synthetic organic chemist to join the Discovery Process Chemistry (DPC) group at our West Point, PA site. The core responsibility of the successful candidate will be to join a team of scientists and contribute to the development of innovative solutions to complex chemistry problems across a diverse portfolio of projects in the discovery phase, from lead identification through candidate selection, with the goal to apply these solutions to facilitate medicinal chemistry research by overcoming synthetic bottlenecks, streamlining SAR analogue synthesis, and providing access to novel chemical space. The position is also responsible for defining scalable synthetic routes and successfully transitioning candidate compounds from discovery into early development, as well as managing supply of Active Pharmaceutical Ingredients (APIs) at varying scales during this period. Close collaboration with chemistry colleagues in Medicinal Chemistry and Process Chemistry, as well as a broad array of other discovery and preclinical research groups, will be expected. As such, subject matter expertise in Medicinal or Process Chemistry is critical. The candidate must be highly self-motivated, possess strong experimental skills, have excellent written and oral communication abilities, collaborate effectively on multidisciplinary teams, and be able to demonstrate flexibility in adapting to change in a fast-paced, dynamic research environment. A demonstrated ability to develop talent through good mentoring skills is an asset as the successful candidate will be expected to grow into the direct supervision of junior colleagues. In addition, the candidate will be expected to remain current with the latest synthetic methodologies, drive innovation, actively apply new concepts to continuously improve Process Research & Development capabilities, and be active in the external scientific community via publications and external presentations. Education: + Ph D in Organic Chemistry Required: + A minimum of 2 years experience with a proven track record of scientific excellence and successful research + Expertise in organic synthesis + Demonstrated creativity and innovation in problem solving + Productivity and efficiency working in the lab + Proven track record of successful research in medicinal and/or process chemistry + Strong written and oral communication skills + Excellent collaboration skills + Ability to contribute on cross-functional teams + Demonstrated external scientific communications by publications and external presentations Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Chemistry_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Associate Principal Scientist – Discovery Process Chemistry_ **Primary Location:** NA-US-PA-West Point **Requisition ID:** _CHE005785_
Merck West Point, PA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. Merck is currently seeking a qualified PET radiochemist within the Department of Translational Biomarkers located at our West Point, PA site in suburban Philadelphia. This innovative team consists of chemists, imaging physiologists, PET modelers and other biological and computational scientists. The group currently has state-of-the-art PET radiochemistry facilities and imaging instrumentation (PET, SPECT, CT, MRI, and optical) for in vivo imaging experimental species. The successful candidate will discover and develop novel PET tracers for use in both preclinical and clinical studies, and direct interactions between the multidisciplinary PET team and preclinical programs for the projects supported. Duties would include: + Responsibility for the design and discovery of novel PET tracers for a variety of targets to support drug discovery and development. + Synthesis of PET tracers to meet a demanding pre-clinical imaging schedule. + Coordination of PET tracer-focused studies + Maintenance and upkeep of laboratory equipment used for PET radiochemistry. + Accurate record keeping for notebooks, equipment logs and research reports. + Contribution to regulatory documents required for clinical PET tracer filings. + Presentation of research results to discovery, pre-clinical and clinical teams, including writing of manuscripts for submission to peer-reviewed journals. + Collaboration with Imaging Department personnel, drug discovery program team leads, and clinical scientists **Education Requirement:** PhD degree in Organic Chemistry or the equivalent **Required Experience and Skills:** + At least 2 year hands on experience with the incorporation of fluorine-18 and carbon-11 into molecules + Directly relevant research experience in PET radiochemistry. + Experience with the discovery and evaluation of novel PET tracers, including the design, synthesis, purification and quality control of small molecule PET tracers for in vivo imaging. + Ability to develop appropriate solutions to overcome challenges associated with the discovery of novel PET tracers. + A strong academic record including publications in peer reviewed journals. + Strong written and oral communication skills. + Interpersonal skills necessary for working in a highly collaborative, cross-functional working environment. + Ability to work independently **Preferred Experience and Skills:** Prefer experience in [11C]methyliodine and [11C]cyanide. Strong interest in understanding biology. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Research Science Generic_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Senior Scientist, Research Science_ **Primary Location:** NA-US-PA-West Point **Requisition ID:** _RES002075_
Merck West Point, PA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its 125-year legacy. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. Under the supervision of a Senior Specialist or Associate Director, is responsible for providing technical manufacturing support in the field of engineering, maintenance and utilities (EMU). Provides day-to-day engineering support for assigned area which may include vaccine bulk manufacturing, filling, lyophilization, packaging, lab operations, and/or mechanical support utilities including power, HVAC, steam, WFI and controlled temperature units. Assigned tasks include support and monitoring of equipment performance and maintenance, propose & develop equipment and facility improvements and troubleshoot process equipment to ensure reliable, compliant and efficient operations. Actively ensures GMP quality, safety, environmental, and operating cost goals are achieved. On occasion, may provide supervisory coverage to ensure supply of a high quality product. Duties include but are not limited to: + Works with Operations, other EM&U engineers, Technology, Maintenance Supervisors and mechanics to maximize capacity and assure efficient, reliable equipment operation in accordance with all GMP, safety and environmental regulations. + Champions the preventive and predictive maintenance program within your area of responsibility, reviews equipment history for reliability concerns, performs root cause analysis, and identifies reliability improvement opportunities and applications for predictive maintenance technologies to reduce maintenance costs. Develops maintenance and repair strategy for bi-annual shutdowns. + Assists/leads Operations, maintenance supervisors, mechanics, automation engineers, process engineers and Quality representatives in troubleshooting equipment problems as well as investigating manufacturing atypical events related to system failure or malfunction. + Serves as the project engineer and manager for small projects including scope development, design support, field execution and commissioning/qualification testing. + Identifies spare parts and stand-by equipment needed to assure maximum capacity and reliability. + Supports maintenance scheduling and planning processes in area of responsibility. + Supports positive safety culture and participates in HAZOP reviews and Safety inspections. Promotes open communications, inclusion and team work. + Authors Standard Operating Procedures or User Manuals and assists in training development for mechanics and supervisors. + Assists in the preparation of process studies, engineering standards, equipment utilization, and profit plan. + Explains and enforces all GMPs, safety, and environmental regulations. + Assist in audits, regulatory inspections and training in the area of responsibility. Education: + Bachelor’s Degree (Engineering or Science) or a 4-Year Engineering Technology Degree or demonstrated equivalent work experience. Required: + Minimum of three (3) years of manufacturing experience or technical support group or equivalent. + Proficiency in the following competencies: empowering leadership, flexibility, motivation, teamwork/collaboration, problem-solving, communication, and computer skills. + Knowledge in the application of engineering standards (i.e. ASME, IEEE, NFPA, CFR 1910, NIST, and/or ANSI). Preferred: + Knowledge of cGMP for pharmaceutical and/or vaccine manufacturing, Lean Six Sigma Methodology, Root Cause Analysis, Failure Mode Effects Analysis. + Knowledge in reliability engineering (including asset life cycle management) as well as Computerized Management Maintenance Systems (CMMS), SAP, PI, Delta V and BAS. + CMRP certification. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need an accommodation for the application process please email us at staffingaadar@merck.com . Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Maintenance/Utilities_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Specialist, Engineering Maintenance & Utilities_ **Primary Location:** NA-US-PA-West Point **Requisition ID:** _MAI000671_
Merck West Point, PA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. The Discovery organization seeks an outstanding candidate to join the Therapeutic Area – Autoimmune and Inflammation Group. This Senior Scientist role will focus on designing and performing experiments using functional in vitro and ex vivo cell-based immunoassays to advance drug discovery research programs from target validation through to lead identification. Broad expertise in immunobiology is required for this role, with preference given to candidates with demonstrated experience in immunology drug discovery and development. The successful candidate will have deep scientific curiosity, excellent oral and written communication skills, the ability to function independently and as part of a team, and be able to work on multiple projects simultaneously. With limited supervision, the role includes developing and optimizing methodologies and assays as well as planning, designing, and executing experiments using good scientific judgment. The position is a hands-on, laboratory based role with no direct reports (individual contributor), but s/he may act as a scientific mentor and coordinate the activities of junior research scientists in support of project objectives. Education: + Ph.D. in immunology, cell biology, pharmacology, or related field with relevant post-doctoral training; 2 years’ experience in the pharmaceutical/biotech industry is preferred (highly qualified candidates with a Master’s degree and 6 years’ industry experience will also be considered). S/he should provide clear evidence of scientific productivity, as evidenced by peer-reviewed publications in top-tier journals and/or by demonstrable achievements in an industrial environment. Required: + Solid training and background in cellular immunology, preferably with area expertise in autoimmunity, immuno-oncology, or infectious disease (including familiarity with associated rodent pre-clinical models). + Ability to independently design, perform and interpret data derived from cellular immune function assays (e.g., differentiation, proliferation, cytotoxicity, cytokine production). + Broad expertise and familiarity with assays and technologies commonly used to assess immune endpoints (e.g., MLR, antigen-specific T/APC cultures; ELISA/ELISPOT, Mesoscale, Luminex; qPCR, NanoString); solid cell line and primary immune cell tissue culture skills. + Experience in multi-parameter flow (FACS) and/or mass (CyTOF) cytometry and proficiency in subsequent downstream data analysis using programs such as FlowJo, FACSDiva, and Cytobank; experience with tissue processing and cell isolation technologies (e.g., Ficoll separation, Miltenyi AutoMACS, FACS sorting). + Ability to organize and communicate complex data sets in a clear and concise manner to key stakeholders from diverse backgrounds. + Ability to contribute at a scientific and strategic level to drug discovery research programs in immunology, including proposal and identification/validation of novel targets. + S/he should be a strong team player with excellent oral and written communication skills and a demonstrated ability to work independently to design and execute experiments, organize and interpret data, troubleshoot, and suggest next steps. Preferred: + Demonstrated project lead experience in an academic or industrial research setting. + Demonstrated experience mentoring and training junior scientists. + Experience with in vivo immune-mechanistic or autoimmune/cancer/infection rodent models and their application towards pharmacological assessment of drug efficacy and mode-of-action; ability to perform (or willingness to learn) basic mouse handling and manipulation techniques (injections, post-mortem tissue collection). + Demonstrable experience with in vitro pharmacology assays involving large or small molecule drugs, e.g., experimental design and replication, titration and potency value determination, etc. + Cell manipulation and engineering towards assay development and target validation (e.g., plasmid/RNAi delivery, CRISPR/Cas9 genomic editing, clonal selection and optimization of reporter cell lines). + Experience directing and coordinating work with external academic/industry partners or with contract research organizations. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . **Search Firm Representatives Please Read Carefully:** Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Biology-Discovery_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Title:** _Senior Scientist_ **Primary Location:** NA-US-MA-Boston **Requisition ID:** _BIO005077_
Merck Boston, MA
Apr 23, 2018
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. This position is critical in Merck’s effort to create a simplified, integrated, user-centric global Quality Management System (QMS) for our human health products with an objective to enable consistently compliant product quality, continuous improvement and effective life cycle management. Act as a cross-functional leader to Simplify, Standardize & Sustain our Compliance Remediation and Support (CRS) department, focusing on API Contract Manufacturing Operations (CMO) sites. Lead development and execution of significant innovation projects driving operational improvements related to Compliance, Remediation and Support at API CMO sites. Support CAPA and inspection readiness processes that are critical to ensure a standardized and sustained QMS. Support alignment for those chapters related to quality/compliance and data integrity, including those that apply to inspection readiness, inspection support and remediation. Ensure robust processes are in place and in use for CAPA management and remediation support. This includes authoring documents, data entry of metrics and CAPA supporting compliance, remediation, and support. Lead during efforts to support inspection remediation and CAPA management processes, demonstrated experience as a lead during Board of Health related inspections. Primary activities include, but are not limited to: + Develop strategy and lead implementation of the CAPA management and remediation process across the API CMO network; define the strategy for global requirements to drive harmonization of processes and systems related to CMO management. + Lead the implementation of QMS requirements related to CAPA Management and Compliance Remediation Support at API CMOs. + Ensure quality requirements are sound and compliant by using insights, experience and judgment to proactively drive and improve the company’s QMS processes and alignment related to GMP and DI requirements. + Provide leadership and technical direction on regulatory GMP requirements to API CMOs. + Initiate, where appropriate, and lead communities of practice to drive best practice sharing and continuous improvements across the MMD network + Develop and proactively identify, investigate and resolve trends and patterns before they impact compliance and supply; define and drive implementation of performance metrics, as appropriate, to measure performance across the API CMO network + Influence and advocate Merck’s position on CRS processes related to HA expectations through a strong network of external connections and effective external engagement. + Anticipate external trends through bench-marking and regulatory intelligence activities and prepare the company proactively for changes and continuous improvements. + Lead, Act, and Support activities to ensure robust processes are in place and in use to maintain the Merck CRS and associated documents. + Lead development and execution of significant innovation projects driving operational improvements; this will require cross-functional support within the Global CRS team and Global QA and External Affairs. Education: + BSc in Life Sciences, Engineering or related relevant discipline Required: + Thorough understanding of regulatory requirements for API, drugs, devices, biologics, including quality risk management and knowledge management. + Minimum of 15 years’ experience in the FDA and/or EU regulated pharmaceutical environment; preferably in an API manufacturing site leading manufacturing and/or quality and/or in Global Quality. + Ability to accurately interpret and apply regulatory expectations for a robust and compliant QMS in an API manufacturing environment. + Strong project management skills. + Capable of working and communicating effectively with all levels of the organization globally + Proven ability to lead and implement multiple projects/tasks simultaneously with competing and/or changing priorities; effective time management + Proven ability to influence effectively without hierarchical authority multi-functional professionals to drive harmonization and proactive compliance + Proven ability to effectively initiate and drive change + Self-motivated with a high degree of ownership and accountability for results Preferred: + MSc or Advanced degree in Life Sciences, Engineering or related relevant discipline preferred + Experience in vaccines, biologics, devices and API regulations preferred + Expertise working with CMOs or Suppliers to drive change and improve compliance. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com . Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster at http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeoc_gina_supplement.pdf Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Job** _Qual Assurance & Ops Generic_ Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. **Other Locations:** _Asia Pacific, Europe, Middle East & Africa, NA-United States_ **_Title:_** _Director, Quality Assurance_ **_Primary Location:_** _NA-US-PA-West Point_ **_Requisition ID:_** _QUA006840_
Merck West Point, PA