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Merck Jobs in Raleigh, NC (NOW HIRING)

Associate Director - Global Engineering Solutions Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range ...

... 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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$64.6K

$107.5K

$159.9K

How much do merck jobs pay per year?

As of Aug 23, 2026, the average yearly pay for merck in Raleigh, NC is $107,458.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,900.00 and $121,500.00 per year, depending on experience, location, and employer.

What is a Merck job?

A Merck job refers to a position at Merck, a global pharmaceutical company focused on healthcare, vaccines, and life sciences. Employees work in various fields, including research, manufacturing, sales, and corporate functions, to develop innovative medicines and therapies. Merck offers diverse career opportunities with competitive benefits, professional development programs, and a commitment to scientific advancement.

What does a typical workday look like for an employee at Merck?

A typical workday at Merck can vary depending on the specific role, but most employees collaborate extensively with multidisciplinary teams to drive projects in research, development, manufacturing, or commercial operations. You may participate in meetings, analyze data, ensure regulatory compliance, and contribute to continuous improvement initiatives. Depending on your department, you might also work with advanced technology tools or engage in problem-solving to address critical challenges. The environment emphasizes teamwork, innovation, and high standards in quality and safety, offering employees the chance to grow and make a meaningful impact on global health.

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

To thrive at Merck, professionals typically need a background in their specific field (such as life sciences, business, or engineering), strong analytical skills, and relevant industry experience or education. Familiarity with tools like SAP, laboratory information management systems, or regulatory compliance platforms is often important, along with certifications such as PMP, Six Sigma, or relevant scientific accreditations. Excellent problem-solving abilities, agility, and collaborative communication skills help individuals excel in Merck’s dynamic and cross-functional teams. These qualifications ensure employees can effectively contribute to cutting-edge healthcare solutions and maintain compliance in a highly regulated, innovation-driven environment.

What are the most commonly searched types of Merck jobs in Raleigh, NC?

The most popular types of Merck jobs in Raleigh, NC are:

What job categories do people searching Merck jobs in Raleigh, NC look for?

The top searched job categories for Merck jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Merck jobs?

Cities near Raleigh, NC with the most Merck job openings:

Infographic showing various Merck job openings in Raleigh, NC as of August 2026, with employment types broken down into 94% Full Time, 5% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $107,458 per year, or $51.7 per hour.

Manufacturing Specialist 1, Drug Product Process

Merck & Co.

Holly Springs, NC • On-site

$70 - $90/hr

Other

Medical, Retirement, PTO

Posted 5 days ago


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Position Overview

Help bring life-changing medicines to patients by ensuring reliable, compliant manufacturing. As a Manufacturing Specialist I, DP, you'll be a hands‑on problem solver and process SME who keeps operations running smoothly in a 24/7 environment-driving documentation excellence, tech transfer readiness, and continuous improvement across Drug Product Finished Goods.

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers

Job Description

About Us We are a high-growth, 24/7 biopharmaceutical manufacturing site focused on delivering high-quality drug products safely and efficiently. Our team values collaboration, learning, and operational excellence. You'll join a global, cross-functional community where your voice matters and your work makes a direct impact on patients.

Responsibilities
  • Support operational readiness during the project phase, including site commissioning and qualification efforts.
  • Troubleshoot process issues and act as a process subject matter expert (SME) for assigned area(s).
  • Coordinate batch planning, including process template creation, import, and the management of Preventative Maintenance (PMs).
  • Own, perform, or drive major documentation updates (including initiating new documents for new processes).
  • Coordinate non-batch activities such as changeover, PMs, and Aseptic Process Simulation (APS).
  • Support MSAT with technology transfer activities within manufacturing.
  • Ensure manufacturing operations adhere to all compliance and safety procedures.
  • Create and update Electronic Batch Records (EBRs) and Paper Batch Records.
  • Manage, perform, initiate, or support change management records, investigations, Corrective and Preventive Actions (CAPAs), and Continuous Improvement (CI) activities.
  • Manage projects, lead execution, and participate in projects within Drug Product Finished Goods.
  • Assist and support inspections and audits to ensure compliance in the manufacturing environment.
  • Assist the Manager with projects and training, as needed.
  • Collaborate effectively in small, cross-functional teams; mentor and guide junior associates.
  • Flexibility with working hours and shift rotation to support a 24/7 manufacturing facility.
Within this role, you'll be successful if you bring:
  • Strong verbal and written communication skills.
  • Strong time management skills.
  • Ability to adapt in a fast‑paced environment, pivot, and adjust plans accordingly.
  • Ability to think critically and demonstrate superior problem‑solving skills.
  • Ability to analyze and troubleshoot simple to moderate system and component‑related issues.
  • Ability to coordinate and facilitate effective small cross‑functional teams.
  • Ability to mentor and guide junior‑level associates.
  • Ability to effectively present information to others.
  • Team‑based attitude and ability to work in a global team environment, build relationships, and communicate effectively with others.
Minimum Qualifications
  • High School Diploma or Equivalent with 9 years of applicable industry experience OR
  • Bachelor's degree with 5 years of applicable industry experience OR
  • Master's degree with 3 years of applicable industry experience OR
  • PhD without experience OR
  • Equivalent Military Experience
Preferred
  • High degree of understanding of operations sequence and cadence of activities in a manufacturing environment.
Benefits
  • Competitive compensation with potential shift differentials for 24/7 operations.
  • Comprehensive health and wellness benefits.
  • Retirement savings and financial wellness support.
  • Paid time off, paid holidays, and flexible scheduling where business needs allow.
  • Professional development, mentorship, and training opportunities.
  • Inclusive, team-oriented culture with global collaboration and opportunities to grow your career.
  • Recognition programs and opportunities to lead and influence process improvements.

We welcome applicants from all backgrounds and experiences. If you're excited to contribute to safe, compliant, and efficient manufacturing-and to grow your impact in a collaborative environment-we'd love to hear from you.

EEO Information

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre‑employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

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