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Merck Contract Jobs (NOW HIRING)

The role also requires effective collaboration with external contract providers as well as ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

... contract. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, leave and disability, employee assistance program, flexible spending accounts, and ...

Analytical Scientist

Saint Louis, MO · On-site

$66K - $99K/yr

In the Analytical Scientist role, you'll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma in St. Louis, MO, and ...

... contract. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, leave and disability, employee assistance program, flexible spending accounts, and ...

Actively collaborate with internal stakeholders and external partners, including contract ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

... contract. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, leave and disability, employee assistance program, flexible spending accounts, and ...

... and at contract manufacturing organizations (CMOs).Provide technical leadership in the ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

... contract. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, leave and disability, employee assistance program, flexible spending accounts, and ...

... contract. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, leave and disability, employee assistance program, flexible spending accounts, and ...

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$60.5K

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How much do merck contract jobs pay per year?

As of Jun 4, 2026, the average yearly pay for merck contract in the United States is $97,205.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,500.00 and $98,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a Merck Contract role, and why are they important?

To thrive in a Merck Contract position, you typically need expertise relevant to the pharmaceutical or life sciences industry, such as a background in biology, chemistry, or business, along with experience in contract management or procurement. Familiarity with contract management systems, regulatory compliance tools, and proficiency in software like SAP or Oracle are often required. Strong negotiation, attention to detail, and effective communication are crucial soft skills for managing agreements and collaborating with stakeholders. These competencies help ensure that contracts are compliant, cost-effective, and aligned with organizational goals.

What types of projects can I expect to work on as a contractor at Merck, and how does this differ from full-time roles?

As a contractor at Merck, you will typically be assigned to project-based work in areas such as research and development, clinical trials, regulatory affairs, or IT systems, depending on your expertise. Contractors often focus on specific deliverables within a defined timeframe and may work alongside full-time employees in cross-functional teams. While you will benefit from Merck's collaborative environment, contractors usually have less involvement in long-term strategic planning or company-wide initiatives compared to permanent staff. This project-based structure offers exposure to diverse challenges and can help expand your professional network within the pharmaceutical industry.

What is a Merck contract?

A Merck contract refers to a formal agreement between Merck, a global pharmaceutical company, and another party such as a supplier, healthcare provider, research organization, or distributor. These contracts outline terms for the supply of products, research collaborations, licensing, or distribution of pharmaceuticals. The agreements ensure compliance with regulations, define responsibilities, and protect the interests of both parties. Merck contracts typically include clauses on confidentiality, intellectual property, dispute resolution, and pricing. Understanding the specifics of a Merck contract is crucial for successful partnerships and regulatory compliance.

What is the difference between Merck Contract vs Merck Clinical Research Associate?

AspectMerck ContractMerck Clinical Research Associate
Required CredentialsTypically requires a bachelor's degree in life sciences or related field, with some roles needing clinical research certificationsRequires a bachelor's degree in life sciences, healthcare, or related field; certifications like CCR or ACRP are common
Work EnvironmentContract-based roles within pharmaceutical or biotech companies, often in office or clinical settingsWorks in clinical trial sites, hospitals, or research facilities, often traveling between sites
Employer & Industry UsageUsed by pharmaceutical companies like Merck for temporary or project-based staffingCommonly employed by pharmaceutical companies, CROs, or research institutions for clinical trial monitoring

In summary, Merck Contract roles are typically temporary positions within the company, focusing on specific projects, while Merck Clinical Research Associates are responsible for monitoring clinical trials, often working at trial sites. Both roles require similar educational backgrounds and certifications, but differ mainly in work setting and job scope.

What cities are hiring for Merck Contract jobs? Cities with the most Merck Contract job openings:
What are the most commonly searched types of Merck jobs? The most popular types of Merck jobs are:
What states have the most Merck Contract jobs? States with the most job openings for Merck Contract jobs include:
Associate Principal Scientist, Analytical R&D

Associate Principal Scientist, Analytical R&D

Merck & Co.

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago


Merck rating

7.8

Company rating: 7.8 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

40th of 71 rated pharmaceutical


Job description

Job DescriptionThe Associate Principal Scientist position will support our Live Virus Vaccines (LVV) -franchise.- This broad role includes 1) working with Analytical Product Leaders (APLs) to develop and implement analytical strategies, with special focus on transition from clinical to commercial stages; 2) driving method alignment and supporting consistent executional excellence across multiple testing laboratories; 3) developing and maintaining a robust assay monitoring effort and -supporting method procedure life cycle management, including automation and/or modernization as applicable.- This position is technical in nature and demonstrated expertise in vaccine analytics is required. The role also requires effective collaboration with external contract providers as well as colleagues in our research laboratories, supply chain, site and global Quality, as well as CMC-Regulatory. This role will be based in West Point, PA and it's a site-based position.

Responsibilities include but are not limited to: Work with APLs to develop and implement the commercialization analytical strategy across testing nodes. Participate in significant investigations across the viral vaccines franchise. Provide Subject Method Expertise to QC analysts and supervisors, assess impact- of proposed changes and deviations.

In partnership with the AWG and network QC labs, support definition of the opportunities for improvement/investment in equipment and technology required to drive assay modernization and implement harmonized network solutions.- This includes working with our Digital manufacturing Division and LMAS team for assay digitization with harmonized data capture. In partnership with the BCR hub, develop short and mid-term strategy for sustainability in BCR inventory and antisera generation needed to support all testing laboratories in the network and connect BCR performance with assay performance as noted above. Provide SME support to APLC gap assessments of key methods to drive improved and sustainable robustness.

Ensure method performance data are presented, discussed and actions developed at analytical working group meetings as appropriate. Collaborate across the internal network, external partners, international governments and/or contract manufacturing and research organizations (CMO/CRO) to ensure uninterrupted supply Escalate key assay challenges to management in a timely and concise manner. Support RTQs, PAI readiness and audit observations - Minimum •Education Requirement and Experience: Bachelor's Degree (BA/BS) with a concentration in sciences with six (6) years of experience working in the field of analytical testing, development, transfer, and/or validation; OR Master's Degree (MA/MS) with a concentration in sciences with four (4) years of experience working in the field of analytical testing, development, transfer, and/or validation; OR PhD with a concentration in sciences with two (2) years of experience working in the field of analytical testing, development, transfer, and/or validation.

- Required Experience and Skills: Demonstrated experience with analytics for commercial vaccine and/or microbiological products. Effective communication and teamwork.- Experience with large molecule GMP testing, including drug substance and drug product stability and release testing. Experience with analytical comparability.

Experience leading a cross-functional team. Strong technical expertise in general large molecule analytical laboratory operations, equipment, and techniques. - Preferred Experience and Skills: Continuous improvement or Project Management training.

Writing or review of technical documents, preferably including regulatory filings (IND, MAA, BLA, PAS, CBE) and inspections with multiple agencies (FDA, EMA, JNDA). Experience with large molecule analytical transfers. Experience with commercial product analytical method changes.

Experience with assay monitoring and trending. VETJOBS#eligableforerpRequired Skills: Adaptability, Analytical Method Development, Assay Development, Biological Assay Development, Cell-Based Assays, Chromatographic Techniques, Cross-Functional Teamwork, External Collaboration, High Resolution Mass Spectrometry (HRMS), Liquid Chromatography-Mass Spectrometry (LC-MS), Mass Spectrometry Analysis, Optimism, Process Analytical Technology (PAT), Protein Analysis, TeamworkPreferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your Rights EEOC GINA Supplement• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment.

We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $142,400.00 - $224,100.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits.- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits .You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee).

The application deadline for this position is stated on this posting. San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully-Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.

-No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.-Employee Status: RegularRelocation:No relocationVISA Sponsorship:No Travel Requirements: 25%Flexible Work Arrangements:Not ApplicableShift:1st - DayValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:06/6/2026 *A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date.

Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R397523 Salary: . Date posted: 05/16/2026


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