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Merck Merck Jobs in Missouri (NOW HIRING)

Merck Group

ERP Senior Project Manager

Saint Louis, MO · On-site

$116K - $159K/yr

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe ...

Merck & Co.

$18.75 - $25.75/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 ...

Merck Group

Staff Software Engineer

Saint Louis, MO · On-site

$110K - $165K/yr

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe ...

Merck & Co.

$18.75 - $25.75/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 ...

Merck Group

Senior Software Engineer

Saint Louis, MO · On-site

$81K - $124K/yr

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe ...

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Merck Merck information

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$62.4K

$103.7K

$154.3K

How much do merck merck jobs pay per year?

As of Jul 31, 2026, the average yearly pay for merck merck in Missouri is $103,691.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,800.00 and $117,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a professional at Merck, and why are they important?

To thrive as a professional at Merck, you typically need a background in life sciences, pharmacy, or a related technical field, along with relevant industry experience. Familiarity with pharmaceutical regulations, clinical trial management systems, and data analysis tools such as SAP or LIMS is highly valued. Strong collaboration, problem-solving abilities, and effective communication are crucial soft skills for success in cross-functional teams. These competencies ensure the ability to drive innovation, maintain compliance, and contribute to the company's mission of improving health outcomes.

What should candidates expect in terms of cross-functional collaboration when working at Merck?

At Merck, employees frequently collaborate across various departments such as research and development, regulatory affairs, marketing, and sales. Team projects often require input from multiple specialties to ensure products meet quality standards and regulatory requirements. This cross-functional teamwork offers exposure to different aspects of the pharmaceutical industry, enhances problem-solving skills, and fosters professional growth through diverse perspectives. Effective communication and adaptability are key to thriving in this collaborative environment.

What is Merck and what does the company do?

Merck is a global pharmaceutical company focused on developing and manufacturing medicines, vaccines, and animal health products. Founded in 1891, Merck (known as MSD outside the United States and Canada) is dedicated to improving health worldwide through innovative research and healthcare solutions. The company operates in areas such as oncology, vaccines, infectious diseases, and cardiometabolic disorders, and is recognized for its contributions to medical research and public health.
What are popular job titles related to Merck Merck jobs in Missouri? For Merck Merck jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Merck Merck jobs in Missouri look for? The top searched job categories for Merck Merck jobs in Missouri are:
What cities in Missouri are hiring for Merck Merck jobs? Cities in Missouri with the most Merck Merck job openings:
Merck Merck jobs near you
Infographic showing various Merck Merck job openings in Missouri as of July 2026, with employment types broken down into 97% Full Time, 2% Part Time, and 1% Temporary. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $103,691 per year, or $49.9 per hour.

Buffer Manufacturing Team Lead - Night Shift

Merck Group

Saint Louis, MO • On-site

$24 - $44/hr

Full-time

Medical, Retirement, PTO

Posted 2 days ago

New

Job description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
The Buffer Manufacturing Team Lead - Night Shift at our Cherokee site, will play a key role within our GMP Operations Systems & Support team (OSS).The Buffer Manufacturing Team Lead is responsible for overseeing and guiding Manufacturing Scientists and Technicians in the preparation and manufacturing of buffers and solutions. This role requires a proactive approach to identifying and resolving issues while fostering a positive and collaborative work environment. The GMP Packaging Lead will drive compliance with all applicable regulations and maintain a safe and efficient work environment. Job duties include:
  • Shift details This role will support 24/7 manufacturing operations and work 12-hour shifts from 6PM - 6:30 AM with 20% shift differential.
  • Lead the buffer formulation team in the execution of cGMP buffer manufacturing.
  • Evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department.
  • Safely perform operations to meet quality expectations.
  • Maintain required training to perform tasks/assignments.
  • Perform routine processes and unit operations.
  • Clean equipment and working areas during and after operations.
  • Support facility functions (e.g., maintain equipment, prepare reagents, restock supplies, waste disposal).
  • Assist with Buffer formulation Schedule and communication with ADC
  • Revise and approve procedures, batch records, and other documentation to ensure compliance with cGMP guidelines.
  • Communicate the status of operations and convey concerns to the supervisor.
  • Provide complete and accurate records consistent with quality guidelines.
  • Ensure all applicable logbooks are completed as required by current procedures.
  • Work cross-functionally with Project Management, Technical Operations, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance.
  • Help with MMF review
  • Participate as needed in quality audits and customer interactions.
  • Improve processes by applying scientific knowledge, experience, and principles, in compliance with change control.
  • Take action to resolve unsafe conditions.
  • Train team members and act as technical consultants.

Physical Attributes:
  • Lift up to 35 lb.
  • Personal protective equipment such as a respirator or chemical protective clothing for extended periods.

Who you are:
Minimum Qualifications:
  • Bachelor's Degree in Chemistry, Biochemistry, Biology, or other scientific discipline
  • 2+ years of experience in GMP manufacturing or operations, in a pharmaceutical or biotechnology environment.

OR
  • High School Diploma or GED
  • 4+ years' experience of experience in GMP manufacturing, in a pharmaceutical or biotechnology environment.

Preferred Qualifications:
  • Excellent problem-solving abilities and a proactive approach to identifying and resolving issues, both process and mechanical.
  • Knowledge of process techniques, unit operations, and safe chemical handling methods.
  • Familiarity with regulatory requirements and industry best practices related to GMP manufacturing, including ICH regulatory and Quality standards.
  • Proficient in SAP, Microsoft Office and other software applications.
  • Strong leadership and interpersonal skills, with the ability to motivate and guide a diverse team.
  • Knowledge of Lean Manufacturing principles and continuous improvement methodologies (OpEx).

RSREMD
Pay Range for this position: $24.00 - $44.00.
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.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Apply