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Merck Co Inc Jobs (NOW HIRING)

MSD

Power Plant - Oper Eng I

Three Rivers, MI · On-site

$39.72 - $49.90/hr

Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway ...

MSD

Product & Business Analysis

West Point, PA · Hybrid

Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway ...

MSD

Operations Technician

Worthington, MN · On-site

... 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 ...

MSD

Product & Business Analysis

Rahway, NJ · Hybrid

Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway ...

MSD

Medical Assistant (Rahway, NJ)

Rahway, NJ · On-site

$18 - $23/hr

... 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 ...

MSD

Off-Shift SPO Technician

West Point, PA · On-site

$17.50 - $23.25/hr

... 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 ...

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Merck Co Inc information

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$66.5K

$110.5K

$164.5K

How much do merck co inc jobs pay per year?

As of Jun 9, 2026, the average yearly pay for merck co inc in the United States is $110,545.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,500.00 and $125,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an employee at Merck & Co., Inc., and why are they important?

To thrive at Merck & Co., Inc., you generally need a strong background in life sciences, pharmaceuticals, or business, along with relevant degrees or industry experience. Familiarity with regulatory requirements, data analysis tools, and pharmaceutical research systems is highly valued. Standout employees demonstrate adaptability, teamwork, and strong communication skills in a global, collaborative environment. These qualities are crucial for driving innovation, ensuring compliance, and delivering impactful healthcare solutions.

What does Merck & Co., Inc. do?

Merck & Co., Inc. is a global pharmaceutical company engaged in the discovery, development, manufacture, and marketing of medicines, vaccines, biologic therapies, and animal health products. The company focuses on several therapeutic areas, including oncology, vaccines, infectious diseases, cardiometabolic disorders, and animal health. Merck is known for its research-driven approach and has developed widely used products such as Keytruda, Gardasil, and Januvia. The company operates in more than 140 countries and is committed to improving health and well-being worldwide.

What is the difference between Merck Co Inc vs Merck Research Scientist?

AspectMerck Co IncMerck Research Scientist
CredentialsBachelor's or higher in life sciences, relevant certificationsAdvanced degree (Master's/PhD), research experience
Work EnvironmentCorporate, manufacturing, and administrative settingsLaboratories, research facilities, clinical trial sites
Employer & Industry UsagePharmaceutical manufacturing and corporate operationsResearch and development within pharmaceutical industry
Common Search & ComparisonCompany overview, employment opportunitiesResearch roles, scientific responsibilities

Merck Co Inc is a large pharmaceutical company involved in manufacturing and corporate functions, while a Merck Research Scientist focuses on scientific research and development within the same industry. The roles differ mainly in responsibilities, required credentials, and work environment, with the Research Scientist engaged in laboratory and research activities.

What is the typical work environment like for employees at Merck & Co., Inc.?

At Merck & Co., Inc., employees often work in a collaborative and fast-paced environment that fosters innovation and continuous learning. Teams are usually cross-functional, allowing for interaction between research, development, regulatory, and commercial departments. The company prioritizes open communication and encourages employees to contribute ideas that drive scientific progress and business success. Depending on the role, you may work on-site at laboratories, in corporate offices, or in hybrid arrangements that combine remote and in-person work.
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Merck Co Inc jobs near you
Infographic showing various Merck Co Inc job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, and 99% Full Time. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $110,545 per year, or $53.1 per hour.
Assoc. Dir, Regional Regulatory Liaison, EEMEA

Assoc. Dir, Regional Regulatory Liaison, EEMEA

MSD

Lebanon, PA • On-site

Full-time

Posted 4 days ago

Job description

Job Description:

*** Please note there is no relocation for this position. The candidate will continue to work from her/his current location.

Lead Regional Product Regulatory Strategy:

  • Responsible to lead regulatory strategy development and execution of pipeline assets for EEMEA region. Supports country prioritization and effective product regulatory submission and approval in a seamless manner through to launch. develops regional/country regulatory strategies for new products filings and Life Cycle Management (LCM) activities (i.e.: new indications, major variations) aligning priorities with business objectives , local regulatory affairs teams and all relevant regional/global stakeholders/governance committees.

  • Is assigned to key pipeline programs, ideally, as of Ph IIa (Proof of Concept, PoC) through to last country launch in region.

  • Serves as single Point of Contact (POC) for specific products for country regulatory teams /HQ teams/regional stakeholders, including Business, Market Access, Medical, etc.

  • Stays updated on our company's pipeline filings, relevant regional and local regulations and guidelines, collects relevant regulatory information (regulatory intelligence) for the region and keeps relevant stakeholders appropriately informed.

Lead for Health Authority questions:

  • Responsible to lead development of the HA responses in

collaboration with the response team, for new products filings and Life Cycle Management (LCM) activities

(i.e.: new indications, major variations).

Coordination of Planning and Execution of Filings:

  • Works with all stakeholders to ensure seamless planning and execution, according to the prioritization, resulting in high quality and compliant on-target regulatory submissions, managing the Health Authority questions, on time approvals, and successful launches. Provides support for New Indications and/or Major Variations that impact launch

Project/Process Support:

  • Leads/Contributes and represent the Region for regional/global projects. Identifies any internal process and/or communication gaps, resolves these or escalates these to regional and global stakeholders for resolution

Qualifications:

  • Must hold a BS degree and/or Master's, Ph.D., degree in pharmacy or other life science.

  • At least 5 years' experience in Regulatory field or equivalent.

  • The candidate should have knowledge/experience in Regulatory Affairs and regulations, registration guidelines and regulatory processes for new product submissions and life cycle management in general and preferably in the intended region.

  • Adapt AI/Digitalization mindset into daily practice

  • Ability to understand/navigate through scientific content

  • Excellent communication skills (both verbal and oral) in English. Experience in global working environment

Required Skills:

Complaint Management, Cross-Functional Teamwork, Pharmaceutical Regulatory Compliance, Prioritization, Process Improvements, Regulatory Affairs Management, Regulatory Management, Regulatory Reporting, Regulatory Strategies, Regulatory Submissions, Stakeholder Engagement

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

06/19/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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