Lab Supervisor 1 - Analytical Development

Biopharma Careers; Rockville (MD); On-site; USD 82,000 - 123,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401(k) matching

Paid time off

Paid holidays

Bonus

Job summary

MilliporeSigma is seeking a laboratory leadership professional in Rockville, MD to ensure GLP/GMP compliant studies and supervise scientific staff. You will direct study conduct, coordinate lab operations, and maintain documentation under strict quality systems.

Responsibilities include scheduling assays, reviewing data for accuracy, and liaising with QA and cross-functional teams to close CAPAs. Strong supervisory skills and GMP knowledge are essential.

Qualifications

• Masters Degree in a Scientific discipline with 1+ years of lab experience.
• Bachelor Degree in a Scientific discipline with 3+ years of lab experience.
• 1+ years of experience leading and training staff in a laboratory setting.

Responsibilities

• Ensure compliance of studies under GxP.
• May act as Study Director for GLP studies.
• Coordinate day-to-day laboratory operations and schedule assays.
• Review study data for accuracy and documentation.
• Liaise with QA and cross-functional teams to close corrective actions.
• Stay current with SOPs and cGMP/regulations.

Skills

Supervisory experience

Analytical chemistry knowledge

HPLC expertise

CE-SDS expertise

cIEF expertise

GMP compliance knowledge

Education

Masters degree in a Scientific discipline

Bachelor's degree in a Scientific discipline

Tools

Compass

Empower

Openlab

Chromeleon

32 Karat

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:

• 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

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;
• 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!