Merck KGaA Posted August 15, 2026

Lab Supervisor 1 - Analytical Development

Rockville, Maryland, United States FULL_TIME
Manufacturing & CMC

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 Lab Supervisor 1, you will oversee the daily management of laboratory conducting a wide variety of assays or tests required to characterize product or material safety. This includes supervision of associate scientists, and/or lab technicians in each lab. This also includes oversight and accountability for quality of work, service delivery, financial targets, and other established lab performance targets. You are responsible for the scientific integrity of technical work performed in manufacturing, and are required to ensure scientific observations, detailed workbooks, and all other documentation fulfill generally accepted (GMP/GLP) professional/industry standards. Requirements also include maintaining a thorough understanding of the company manufacturing and testing services, technical principles, and applications as they apply to your position. Specific responsibilities include:

Responsible for compliance of studies under the principles of GxP.

May act as Study Director with responsibility for the scientific conduct of GLP studies.

May act as the study management/ responsible person on the release of test results in a GMP study.

Document scientific observations and coordinate all activities associated with day-to-day laboratory operations.

Schedule the conduct of assays by lab staff and coordinate the scheduling samples to be tested.

Ensure the necessary paperwork is received to facilitate on time lab initiation of studies.

Review study data for accuracy, adherence to compliance and completeness of documentation.

Conduct thorough scientific investigations to determine the root cause for each deviation and nonconformance.  Document all aspects of the investigation in a timely manner.

Liaise with Quality Assurance and appropriate cross-functional departmental areas to close the events and corrective actions identified during GxP laboratory testing.

Stay current with SOPs and regulations (cGMP and GLP).

Periodically evaluate laboratory procedures, system controls and technical documentation such as SOPs and batch records to ensure compliance.

Manage the use and maintenance of scientific equipment and instrumentation, computer systems; Ensure that they are kept in a calibrated / validated state and part 11 compliant.

Assist in site visits (Technical and QA), complete client requests and addressing site visit/ audit findings in a timely manner.

Participate in conference calls and anticipate/ address client questions as appropriate.

Provide direct supervision to Associate Scientists and/or Laboratory Assistants.  Meet with direct reports to set goals, conduct regular one-on-one discussions with employees, ensure development plans are in place for all employees, address personnel issues promptly, interview and hire new candidates and complete performance reviews fairly and on-time.

Act as point of contact for departmental training, ensuring training modules are up to date and training matrix reflects staff capabilities.

Participate in division-wide initiatives including Quality systems improvements, trans-divisional SOPs revisions, Lean projects, etc.

Perform other duties and responsibilities as appropriate or required.

Who You Are

Minimum Qualifications:

Masters Degree in a Scientific discipline (e.g., Biology, Chemistry, Microbiology) with 1+ years of lab experience.

OR

Bachelors Degree in a Scientific discipline (e.g., Biology, Chemistry, Microbiology) with 3+ years of lab experience.

1+ years of experience leading and training staff in a laboratory setting.

Preferred Qualifications:

Supervisory/team lead experience in a laboratory setting or scientific industry.

Working knowledge of analytical chemistry applicable to Quality Control testing within the Product Characterization lab.

Expertise in HPLC, CE-SDS, and cIEF.

Strong knowledge of GMP practices, compendial regulations, quality assurance, and compliance standards.

Proficient with Compass, Empower, Openlab, Chromeleon, and 32 Karat software systems.

Excellent oral and written communication skills that have been demonstrated through presentations/seminars, oversight of projects, implementation of new services, etc.

Excellent time management skills.

Highly collaborative yet able to succeed independently.

Demonstrate a high level of initiative and leadership capabilities.

Effective supervisory, coaching, and training skills for complex and highly technical work

Pay Range for this position: $81,900- $122,800

Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career  level , and other job-related factors.  This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses.

RSREMD

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
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Rockville, Maryland, 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 1793 comparable Manufacturing & CMC roles across 130 biopharma companies.

1793Comparable roles tracked
1703Currently active
130Companies hiring similar roles
47Countries represented

Salary context

526 of 1793 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $81,900/yr – $122,800/yr
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Technical Operator, Packaging - 2nd Shift · Mylan Technologies, Inc. $37,000/yr – $800,000/yr
Peer group range $0 – $418,500 (median $135,233)

Where these roles are based

Top locations among the 1793 comparable roles

United States894
India117
Germany101
France74
Singapore70
Ireland64

+ 41 more countries

Seniority mix

789 of 1793 peers have a known seniority level

Senior258
Manager203
Associate82
Principal82
Director62
Associate Director61
Senior Director25
Intern/Fellow/Postdoc11
Executive/VP5

Therapeutic area mix

6 of 1793 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease4
Oncology1
Rare Disease1

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.

40%similar
AstraZeneca New Haven, Connecticut, United States of America
Same function Same country
40%similar
AstraZeneca Cambridge, Massachusetts, United States of America Director
Same function Same country
40%similar
AstraZeneca New Haven, Connecticut, United States of America
Same function Same country
40%similar
40%similar
Lilly Boston, Massachusetts, United States of America Associate
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function 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.

40%
Scientist II, LC Development, Biologics Analytical Development
AstraZeneca · New Haven, Connecticut, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
40%
Director, Global Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC), Platform Innovation – Synthetic Peptides and Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Senior/Principal Scientist, Bioprocess Purification Development
Lilly · Indianapolis, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
40%
Senior Principal Scientist - Bioanalytical Research
Lilly · Louisville, Colorado, United States of America · Principal
Function Therapeutic area Seniority Country
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.