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Senior Specialist Merck Jobs (NOW HIRING)

The senior specialist is responsible for automation system performance, compliance, reliability ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

$117K - $184K/yr

Sr. Specialist -Discovery Process Chemistry (P3) The Discovery Process Chemistry group within the ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

New

$106 - $167/hr

The Customer Contract Management (CCM) Contract Analyst (Senior Specialist) is responsible for ... Learn more about your rights, including under California, Colorado and other US State Acts Merck ...

New

The Senior Specialist, Engineering, will be responsible for support of production of live virus vaccines within bulk vaccine production and/or final formulation and filling operations. This engineer ...

$129K - $203K/yr

The senior specialist should demonstrate collaborative work spirit and good communication skills ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

$117K - $184K/yr

The Senior Specialist, Engineering, will be responsible for support of production of live virus ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Senior Specialist, Engineering

Rahway, NJ · On-site

$117K - $184K/yr

Sr. Specialist -Discovery Process Chemistry (P3) The Discovery Process Chemistry group within the ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

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Senior Specialist Merck information

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$29K

$93.6K

$140K

How much do senior specialist merck jobs pay per year?

As of Aug 22, 2026, the average yearly pay for senior specialist merck in the United States is $93,575.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $121,000.00 per year, depending on experience, location, and employer.

What does a senior specialist at Merck do?

A Senior Specialist at Merck is typically responsible for providing advanced expertise in a specific area such as research, quality assurance, regulatory affairs, or IT. They lead key projects, collaborate with cross-functional teams, and ensure compliance with industry standards and company policies. Senior Specialists also mentor junior staff, contribute to process improvements, and help drive innovation within their department. Their role is critical in supporting Merck’s mission to discover, develop, and deliver innovative medicines and vaccines.

What skills and qualifications are needed to thrive as a senior specialist at Merck?

To thrive as a Senior Specialist at Merck, you typically need advanced expertise in your specific scientific or business field, a relevant bachelor’s or master’s degree, and significant industry experience. Familiarity with industry-standard software, data analysis tools, and knowledge of pharmaceutical regulations or compliance systems is often required. Strong project management, communication, and problem-solving skills set exceptional candidates apart in this role. These capabilities are crucial for effectively driving projects, ensuring regulatory compliance, and collaborating across teams in a dynamic pharmaceutical environment.

How does a senior specialist at Merck typically collaborate with cross-functional teams to drive project success?

Senior Specialists at Merck often work closely with cross-functional teams that may include scientists, regulatory affairs, project managers, and commercial colleagues. They provide subject matter expertise and ensure that projects align with both strategic objectives and compliance standards. Collaboration is key, involving regular meetings, status updates, and shared project management tools to track progress and address challenges. This dynamic environment fosters strong communication skills and the ability to adapt to changing priorities, making the role both challenging and rewarding.

What is the difference between Senior Specialist Merck vs Senior Scientist Merck?

AspectSenior Specialist MerckSenior Scientist Merck
Required CredentialsBachelor's or Master's degree in relevant field, certifications may varyMaster's or PhD in relevant scientific discipline, often with research experience
Work EnvironmentRegulatory, quality assurance, or process-focused teams within pharmaceutical manufacturingResearch and development labs, scientific research, and experimental design
Employer & Industry UsageCommonly used in pharmaceutical, biotech, and healthcare companies like MerckPrimarily used in research-focused roles within similar industries

While both roles are integral to Merck's operations, the Senior Specialist typically focuses on regulatory compliance, quality, or process management, whereas the Senior Scientist is more research-oriented, involved in scientific experiments and development. The choice depends on whether the role emphasizes regulatory/quality expertise or scientific research.

What cities are hiring for Senior Specialist Merck jobs?

Cities with the most Senior Specialist Merck job openings:

What states have the most Senior Specialist Merck jobs?

States with the most job openings for Senior Specialist Merck jobs include:

Infographic showing various Senior Specialist Merck job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $93,575 per year, or $45 per hour.

Senior Specialist, Quantitative Pharmacology and Pharmacometrics - Cardiometabolic and Ophthalm[...]

MSD Malaysia

West Point, PA • On-site

$129 - $203/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


Job description

Job Description The Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's Research Laboratories in West Point, PA / Rahway, NJ is seeking a curious and collaborative Senior Scientist to support our rapidly expanding cardiometabolic and ophthalmology pipelines. As a senior specialist you will be part of a cross-functional teams of experienced scientists to discover and develop novel therapeutic agents of various modalities for cardiometabolic and ophthalmic diseases. The senior specialist is a skilled quantitative scientist, with a good understanding of the strategic elements of drug discovery and development. The senior specialist should demonstrate collaborative work spirit and good communication skills. Within QP2, you have a unique opportunity to accelerate your professional career as a quantitative drug developer taking advantage of our end-to-end pipeline support in one of the world’s most research-intensive biopharmaceutical companies.

Responsibilities:
  • Contribute to the development of model-based strategies (translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within and across development programs and/or departments, to inform and optimize drug discovery and all phases of drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions.
  • Represent QP2 on cardiometabolic and ophthalmology discovery, early clinical development and late clinical development teams, leveraging quantitative approaches to drive streamlined development of programs within our growing portfolio.
  • Collaborate with other functional areas, as well as with external vendors and partners, on activities related to study design, protocol development, study execution, reporting and interpretation of data.
Required:
  • A Ph.D. or equivalent degree OR a PharmD or equivalent degree with at least 2 years of experience OR an MS or equivalent degree with at least 4 years of experience, where “experience” means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development, regulatory agency, or academia.
  • Educational background in biopharmaceutics, pharmaceutical sciences, pharmacometrics, chemical/biomedical engineering, or a related field.
  • Experience in performing population PK, PK/PD analyses using standard pharmacometrics software (e.g. NONMEM, Monolix, Phoenix, etc.).
  • Good written and verbal communication, interdisciplinary collaboration, and problem scoping and planning.
Preferred:
  • Knowledge in cardiometabolic and/or ophthalmology clinical drug development programs
  • Skills in experimental design, mathematical problem solving, critical data analysis/interpretation, and statistics.
  • Scientific understanding of biopharmaceutical and ADME properties of small molecules and/or biologics
Required Skills:
  • Clinical Study Design, Clinical Trial Designs, Clinical Trials, Database Design, Data Engineering, Data Modeling, Data Science, Data Visualization, Interdisciplinary Collaboration, Machine Learning (ML), Pharmacodynamics, Pharmacokinetics, Pharmacotherapeutics, Waterfall Model
US and Puerto Rico Residents Only:

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: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 08/28/2026 *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.

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

The salary range for this role is $129,000.00 - $203,100.00 This 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.

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

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