Merck KGaA Posted August 15, 2026

Associate Production Scientist, Projects

Milwaukee, Wisconsin, United States FULL_TIME
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Merck KGaA is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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:

As an Associate Production Scientist specializing in Safety, Quality, and Technical Writing, you will play a pivotal role in driving continuous improvement initiatives within our organization. The hours for this position are 7:00am–3:30pm Monday-Friday, though it may involve flexible hours and occasional hybrid work depending on business needs. More specific responsibilities include:

Safety: Conduct comprehensive risk assessments and implement measures to enhance laboratory and operational safety.

Develop and implement safety protocols, ensuring compliance with industry regulations and best practices.

Collaborate with cross-functional teams to establish and maintain a safety-first culture within the organization.

Quality: Design, implement, and optimize quality control procedures to uphold and improve product quality.

Investigate and resolve complex process quality issues, implementing corrective and preventive actions.

Comply with change control procedures. Participate as needed in quality & safety audits.

Technical Writing: Create and maintain detailed technical documentation, including standard operating procedures (SOPs), work instructions, and safety manuals.

Communicate complex scientific concepts in a clear and concise manner for diverse audiences, including regulatory agencies and internal stakeholders.

Review and update documentation regularly to reflect process changes and improvements.

Project Management: Lead and participate in cross-functional project teams focused on safety, quality, and process improvement initiatives.

Collaborate with R&D, production, packaging engineering, planning, and regulatory affairs teams to integrate safety and quality considerations into new product development.

Other duties as assigned by manager.

Perform public speaking as needed, including monthly safety meetings.

Perform and interpret analytical evaluations of products and intermediates.

Participation in Medical Emergency Response Team and/or Emergency Spill Response Team.

Provide complete and accurate records consistent with quality guidelines (GDP).Contribute to support functions of the department (e.g., maintain equipment, prepare reagents, restock lab supplies, perform waste disposal, design & build chemical packaging apparatus, create & maintain work instructions, troubleshoot process/equipment issues, etc.).

 

Physical Attributes:

Chemical environment - perform tasks while wearing personal protective equipment such as respirator or chemical-protective clothing for extended periods.

Occasional lifting and pushing of up to 50 pounds.

 

Who You Are

Minimum Qualifications:

Bachelor’s Degree in Chemistry, Biology, or other Life Science discipline

1+ years of professional lab experience or in operations/manufacturing

 

Preferred Qualifications:

Strong background in chemistry, experimental design, and/or lab/manufacturing safety.

Independent lab research, and project management experience.

Familiar with laboratory instruments and production equipment.

Knowledge of process techniques and unit operations.

Familiar with analytical techniques and equipment.

Communication skills, both oral and written.

Ability to use various computer programs, including Microsoft Office, inventory control software (e.g. SAP), and quality management software.

Basic-to-intermediate mechanical skills (i.e., use of basic hand tools).

Troubleshooting skills.

Interpersonal skills.

Organizational skills.

Knowledge of ISO Quality standards.

Pay Range for this position: $27-$48/hour

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!

Job details

Seniority
Associate
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Milwaukee, Wisconsin, United States
Employment type
FULL_TIME

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 565 comparable Associate Manufacturing & CMC roles across 80 biopharma companies.

565Comparable roles tracked
517Currently active
80Companies hiring similar roles
32Countries represented

Salary context

124 of 565 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $27/hr – $48/hr (≈ $56,160–$99,840/yr)
Lowest disclosed · Production Associate · Merck KGaA $17/hr – $27/hr (≈ $35,360–$56,160/yr)
Highest disclosed · Regional Manager - Megasys · Merck KGaA $220,000/yr – $250,000/yr
Peer group range $45,760 – $235,000 (median $123,700)

Where these roles are based

Top locations among the 565 comparable roles

United States321
India62
Germany23
France20
Ireland14
United Kingdom13

+ 26 more countries

Seniority mix

565 of 565 peers have a known seniority level

Manager265
Associate153
Intern/Fellow/Postdoc147

Therapeutic area mix

8 of 565 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease6
Rare Disease2

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority Same country
60%similar
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Same function Same seniority Same country
60%similar
Devens Devens, United States Associate
Same function Same seniority Same country
60%similar
Celgene - Summit (Corp) Summit West, United States Associate
Same function Same seniority Same country
60%similar
Bayer Pittsburgh Heilman, United States Associate
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60%similar
Biogen Research Triangle Park, United States Associate
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.