Jobs at Merck

6,682 open positions

Merck & Co., Inc. is a global pharmaceutical and biotech company headquartered in Kenilworth, New Jersey. Beyond drugs like Keytruda and Januvia, Merck has expanded into digital health, AI‑driven drug discovery, and precision medicine. The company’s research labs integrate advanced data analytics to accelerate clinical trials and develop next‑generation therapeutics.

Merck’s tech hiring focuses on data science, software engineering, AI research, and product management across its R&D, manufacturing, and commercial divisions. Candidates can expect algorithm‑based coding challenges, domain‑specific case studies, and collaborative teamwork that reflects Merck’s emphasis on scientific rigor and patient impact. The interview process typically includes a technical screen, a live coding session, and a behavioral panel that evaluates problem‑solving, communication, and ethical decision‑making.

Job Transparency’s listings for Merck provide exact salary ranges, bonus eligibility, and real employee sentiment scores based on thousands of anonymous reviews. By comparing the listed compensation with industry benchmarks and reading candid feedback about workplace culture, applicants can negotiate confidently and choose roles that align with their career goals.

Associate Director, Third Party Quality Management Drug Product (Hybrid)

Company: Merck

Location: Rahway, NJ

Posted Dec 04, 2024

The job posting is for an Associate Director, Third Party Quality Management Drug Product. The role involves leading quality relationships with contract manufacturing organizations, negotiating agreements, conducting audits, and supporting product development teams. The ideal candidate should have a minimum of 5 years in pharmaceutical drug product manufacturing and 10 years in biopharmaceuticals. They should be able to plan and facilitate high-risk process reviews, identify trends, and interpret complex regulatory requirements. Preferred experience includes work with medical devices and combination products, and engagement with small and large molecule drug development programs.

Associate Director, Regulatory Affairs-CMC

Company: Merck

Location: Williamsport, PA

Posted Dec 04, 2024

The CMC Operations Associate Director will play a crucial role in the Global Regulatory Affairs & Clinical Safety (GRACS) CMC Operations team. They will be responsible for delivering regulatory tools, systems, and processes that support CMC regulatory operations throughout the product lifecycle. Key responsibilities include Change Control Management, Regulatory Submission Planning, Content Authoring, and Health Registration Management. The ideal candidate will collaborate with various stakeholders, gather and analyze business requirements, and translate these into technical specifications. They will also support operations documentation, create and maintain comprehensive records, and work on process optimization. The role requires strong leadership, problem-solving skills, and the ability to work in ambiguous situations. A Bachelor's degree in a relevant discipline and a minimum of 10 years of pharmaceutical industry experience are required.

Director, Quantitative Pharmacology and Pharmacometrics - Immune/Oncology - Hybrid

Company: Merck

Location: Rahway, NJ

Posted Dec 04, 2024

The text describes a job posting for a Director position in the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team. The role involves leading drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs. The Director will work closely with cross-functional scientists, develop strategies for quantitative analyses, and maintain a comprehensive understanding of global regulatory expectations. The ideal candidate should have a Ph.D. with at least seven years of experience in PKPD, pharmacometrics, mathematics, statistics, or chemical/biomedical engineering. Required skills include proficiency in R, NONMEM, MATLAB, Monolix, and strong communication skills.

Associate Director, Safety & Environment

Company: Merck

Location: Rahway, NJ

Posted Dec 04, 2024

This job posting is for a crucial role in the EHS Operational Excellence team, focusing on data strategy, governance, and optimization of EHS business processes. The role involves leading the development of EHS data strategy, optimizing processes, evaluating digital tools, developing critical metrics, and creating a training strategy. The ideal candidate should have a Bachelor's degree in environmental, safety, or related field, and 7+ years of progressive EHS experience. Strong analytical skills, problem-solving ability, project management skills, and excellent communication skills are required. The role is pivotal in ensuring EHS programs are data-driven, aligned with the company's mission, and reflective of its commitment to safety and environmental stewardship.

Senior Specialist, Strategic Programs Corporate & Site Services (CSS)- Hybrid

Company: Merck

Location: Rahway, NJ

Posted Dec 04, 2024

This job description outlines a Senior Specialist role within Corporate & Site Services (CSS), emphasizing strategic sourcing, project management, and cross-functional collaboration. It highlights required skills in procurement, data analysis, and leadership, while also detailing hybrid work arrangements and commitment to diversity and inclusion.

Off-Shift SPO Electro-Mechanical Technician

Company: Merck

Location: Spring House, PA

Posted Dec 04, 2024

The job posting is for a Growth and Improvement minded SPO Technician | Level 1 position at a rapidly growing pharmaceutical manufacturer. The role involves working in manufacturing plants with a focus on safety, quality, and continuous improvement. Key responsibilities include formulating bulk product and culture media, cleaning and sterilizing equipment, operating filling and packaging equipment, and maintaining documentation. The ideal candidate should have a high school diploma or equivalent, an Associate degree in Applied Science or equivalent, or relevant military or maintenance experience. They should also possess strong communication skills, be able to work independently and as part of a team, and have experience in mechanical, electronic, electrical, and pneumatic/hydraulic troubleshooting and repairs.

Associate Director, Project Management - Drug Development (Hybrid)

Company: Merck

Location: Spring House, PA

Posted Dec 04, 2024

The GPAM Associate Director, Project Manager, is a crucial member of Early Drug Development and/or Late Drug Development Teams. They develop strategies and execute drug and vaccine development efforts, progressing the R&D pipeline. The role requires managing complex drug development projects, driving cross-functional teams, and leading by influence. The Associate Director is expected to contribute to business process improvement and talent development in GPAM. They must have a Bachelor's degree, preferably in a scientific discipline, and at least five years of project management experience, preferably in the pharmaceutical/biotech industry. Advanced degrees, clinical drug development experience, and project management certifications are preferred. The role involves minimal travel and offers a competitive salary range of $135,500.00 - $213,400.00.

Senior Specialist, Global Expert Management and Strategy (GEMS)

Company: Merck

Location: Rahway, NJ

Posted Dec 04, 2024

The Senior Specialist Global Professional Engagement role is part of GEMS Consulting & Medical Education within V&I Global Medical and Value Capabilities (GMVC). The role involves planning and executing global advisory boards, expert input programs, and ex-US global medical education programs. The individual must be detail-oriented, strategic, and capable of developing comprehensive assessments. They will manage end-to-end therapeutic focused expert input activities and medical education programs, ensuring alignment with strategic plans, scientific platforms, and market needs. The role requires a Bachelor's degree, 5+ years of pharmaceutical industry experience, and strong project management skills.

Senior Statistical Programmer, Late Stage Development, Oncology (Hybrid)

Company: Merck

Location: Spring House, PA

Posted Dec 04, 2024

BARDS, a distinguished department within the company's R&D division, seeks a quantitative scientist for late-stage drug/vaccine clinical development projects. The role involves leading statistical programming activities, developing and executing analysis and reporting deliverables, and collaborating with stakeholders. The ideal candidate should have a BA/BS or MS in a relevant field with substantial SAS programming experience in a clinical trial environment. Key skills include effective interpersonal and communication abilities, project leadership, and expertise in SAS and clinical trial programming. Preferred experience includes regulatory application submission experience and process compliance assurance.

Executive Director, Data Management and Governance

Company: Merck

Location: Rahway, NJ

Posted Dec 04, 2024

The Digital Data Management and Governance Product Line Lead is a senior leadership role in Digital Services, responsible for establishing and driving data management strategy. This role involves strategic leadership, product strategy definition, and ensuring high-quality master data with fit-for-purpose technology. The Product Line Lead sets the vision for master data management platforms, owns end-to-end responsibility for all products, and leads the Manufacturing data quality function. They are accountable for value delivery, forging partnerships with key stakeholders, and managing budget and total cost of ownership. The ideal candidate should have extensive experience in biopharmaceutical industry, digital and leadership experience, and strong skills in data management, data governance, data quality, and data literacy.

Associé marketing, oncologie / Marketing Associate, Oncology

Company: Merck

Location: Kirkland, Canada

Posted Dec 04, 2024

The Marketing Associate, Oncology role involves supporting the Oncology Business Unit with tactical and operational tasks, including developing strategic plans, assisting with new indication launches, managing budgets, and leading projects. The ideal candidate should have strong communication, teamwork, and problem-solving skills, with a bachelor's degree in Science or Business. Bilingualism in French and English is required. The role offers a hybrid work arrangement, combining remote work and in-person work at the Kirkland Head Office.

Specialist, Logistics - Export Specialist (Remote)

Company: Merck

Location: Spring House, PA

Posted Dec 04, 2024

The job description is for a role responsible for ensuring U.S. exports from Company Research Laboratories comply with U.S. regulations and Company standards. The position involves working with various intercompany partners, performing export transactions in a Global Trade Management System, and maintaining knowledge of U.S. export regulations. Qualifications include a Bachelor's degree in International Trade or International Business, 5+ years of functional expertise, and experience with Global Trade Management Systems.

Frequently Asked Questions

What’s it like to work at Merck?
Working at Merck means collaborating with scientists, clinicians, and data experts to deliver life‑changing therapies. Employees value the company’s commitment to research excellence, benefit packages that include health, wellness, and retirement plans, and a culture that encourages continuous learning. Leadership promotes cross‑functional projects, providing opportunities to impact product development from discovery to commercialization.
What tech positions are available at Merck?
Merck hires a wide range of tech roles: Data Scientists, Machine Learning Engineers, Software Engineers (backend, frontend, full stack), DevOps Specialists, Cloud Architects, AI Researchers, Product Managers, Clinical Informatics Analysts, and Cybersecurity Engineers. Positions span R&D labs, manufacturing IT, and commercial digital platforms like the Merck Digital Health Group.
How can I stand out as a Merck applicant?
Show domain‑specific expertise—demonstrate knowledge of bioinformatics, clinical data, or pharma software. Build a portfolio with projects that solve real‑world problems, such as analyzing clinical trial data or optimizing supply‑chain logistics. During interviews, prepare for both coding challenges and scenario‑based questions that test ethical decision‑making in a regulated industry. Highlight your ability to collaborate across disciplines and your commitment to innovation and patient outcomes.

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