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How much do merck manufacturing jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for merck manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What is Merck Manufacturing?

Merck Manufacturing refers to the division of Merck & Co., Inc. responsible for the production and supply of medicines, vaccines, and other health products. This team manages the end-to-end manufacturing process, ensuring that products are made safely, efficiently, and to the highest quality standards. Merck Manufacturing includes roles in process development, quality assurance, supply chain management, and operations, supporting global healthcare needs. Their work is essential to delivering Merck's products to patients around the world.

What are the key skills and qualifications needed to thrive as a Merck Manufacturing professional?

To thrive in Merck Manufacturing, you need a strong background in life sciences or engineering, experience in GMP-regulated environments, and often a relevant degree such as chemical engineering, biology, or pharmaceutical sciences. Familiarity with manufacturing execution systems (MES), quality management software, and regulatory compliance certifications like Six Sigma or Lean are often required. Attention to detail, problem-solving abilities, and teamwork are essential soft skills to excel in this role. These skills ensure production quality, regulatory compliance, and efficient collaboration in delivering safe and effective pharmaceuticals.

What are some common challenges faced by professionals working in Merck Manufacturing, and how can they be addressed?

One common challenge in Merck Manufacturing is maintaining high quality and compliance standards while meeting production targets. Employees often need to adapt quickly to evolving regulatory requirements and new technologies. Effective communication and collaboration with cross-functional teams, such as quality assurance and engineering, are essential for overcoming these challenges. Additionally, Merck provides ongoing training and resources to help manufacturing professionals stay up-to-date and succeed in their roles.

What is the difference between Merck Manufacturing vs Merck Quality Control?

AspectMerck ManufacturingMerck Quality Control
Primary RoleOversees production processes, equipment, and manufacturing operationsEnsures product quality through testing, inspection, and validation
Required CertificationsManufacturing certifications, GMP trainingQuality assurance certifications, GMP training
Work EnvironmentFactories, production lines, manufacturing plantsLaboratories, testing facilities, quality labs
Industry UsageUsed in pharmaceutical manufacturing settingsUsed in quality assurance and control departments

Merck Manufacturing focuses on the production and assembly of pharmaceutical products, ensuring manufacturing efficiency and compliance. In contrast, Merck Quality Control emphasizes testing and verifying product quality to meet safety standards. Both roles are essential in the pharmaceutical industry and often work closely to ensure high-quality products reach consumers.

What cities are hiring for Merck Manufacturing jobs?

Cities with the most Merck Manufacturing job openings:

What states have the most Merck Manufacturing jobs?

States with the most job openings for Merck Manufacturing jobs include:

What job categories do people searching Merck Manufacturing jobs look for?

The top searched job categories for Merck Manufacturing jobs are:

Merck Manufacturing jobs near you
Infographic showing various Merck Manufacturing job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

Manufacturing Supervisor Weekend Day Shift

Merck Group

Madison, WI • On-site

$85K - $136K/yr

Full-time

Medical, Retirement, PTO

Posted 14 days ago

Job description

Work Location: Madison, Wisconsin
Shift:
Department: LS-SC-UYWMC Madison Manufacturing
Hiring Manager: Ben Simoni
This information is for internals only. Please do not share outside of the organization.
Your Role:
The Manufacturing Supervisor position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API's) according to current Good Manufacturing Practice (cGMP) requirements.
This position is for B shift. (Thursday - Sunday 6:30am - 7:00pm, then Friday - Sunday 6:30am - 7:00pm)
  • Supervise, train, and motivate staff; lead shifts to meet deadlines, enforce expectations, and take corrective actions when necessary
  • Maintain safe, clean work environments and model ethical, professional behavior as a representative for customers and vendors
  • Ensure cGMP documentation accuracy, interpret in-process data, and provide secondary data review during off-shifts
  • Oversee and assist in API and intermediate manufacturing, serving as a primary operator and ensuring effective equipment operation and troubleshooting
  • Apply strong knowledge of MilliporeSigma procedures, synthetic/process chemistry, and EDMS system to support production activities
  • Author, review, and train staff on batch records, SOPs, and other written procedures while ensuring compliance with FDA, OSHA, EPA, DOT, and other regulations
  • Coordinate project flow, scale-up, and tech transfer between departments, providing status updates and generating cost models for quotes
  • Conduct employee training, performance reviews, recruitment, and cross-training to build effective teams within the production department
  • Identify production gaps, drive continuous improvement initiatives, and remain available for emergency support

Physical Attributes:
  • Stand for long periods of time.
  • Lift and move up to 50 pounds with the assistance of equipment or teammates as necessary.
  • Operate hand tools, calculators, and weighing / measuring devices

Employee will adhere to the GMP requirements defined within 21 CFR parts 210 &211, 820, ICH Q7, Safety standards set under ISO 14001 & 45001. This position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API's) according to current Good Manufacturing Practice (cGMP) requirements. The role of Manufacturing Supervisor is primarily focused on ensuring manufacturing staff execute required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing existing production procedures, updating supporting documents, and maintaining the safety and quality of the manufacturing environment.
Who You Are
Minimum Qualifications:
  • Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering or other Life Science discipline.
  • 2+ years of work experience in chemical or pharmaceutical manufacturing.
  • 2+ years of manager/supervisor experience

Preferred Qualifications:
  • Ability to read and understand written protocols
  • Ability to demonstrate leadership skills and lead by example
  • Strong computer literacy (Microsoft Office and Outlook tools, Electronic Document Management Systems, etc.)
  • Effective oral and written communication skills
  • Mechanical and technical aptitude
  • Strong mathematical skills
  • Possess a high degree of internal motivation
  • Ability to multi-task while paying close attention to detail

Pay Range for this position: $85,000-$136,800.
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here
RSREMD
RSREMD
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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