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Upstream Manufacturing Associate Scientist - Cell culture

Job in St. Louis, Saint Louis, St. Louis city, Missouri, 63105, USA
Listing for: The businesses of Merck KGaA, Darmstadt, Germany
Full Time position
Listed on 2026-01-12
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 23 - 42 USD Hourly USD 23.00 42.00 HOUR
Job Description & How to Apply Below
Location: St. Louis

Work Location:

St. Louis, Missouri

Shift: No
Department: LS-SC-PMLPCCB Cell Marque Upstream
Recruiter:
Guadalupe Barragan

Hiring Manager:
Tara Giebe

Your Role

The Upstream Manufacturing Associate Scientist performs laboratory operations required to manufacture and monitor antibody production including cell culture, bioreactors, transient transfection, ELISA, and tissue staining according to established manufacturing procedures with some supervision; completes required tasks per standard operating procedures involving laboratory techniques, calculations, material measurements, operation of laboratory equipment, and record keeping as necessary.

  • Perform laboratory operations required to manufacture and monitor antibody production including cell culture, bioreactors, transient transfection, ELISA, and tissue staining according to established manufacturing procedures.
  • Ensure compliance with cGMP, FDA, ISO, and other applicable regulatory standards (OSHA, USDA, EPA), meeting all quality requirements and deadlines.
  • Support the development, documentation, and continuous improvement of lab procedures and manufacturing processes to maintain regulatory compliance.
  • Assist in the development and validation of new assays, instrumentation, and manufacturing workflows; support staff training as needed.
  • Maintain accurate records using local ERP systems and ensure proper documentation of all manufacturing processes.
  • Perform routine equipment maintenance, manage inventory of chemicals and supplies, and contribute to general lab cleanliness.
  • Escalate non-conformances, participate in investigations, and proactively seek opportunities to improve productivity, quality, and compliance.
  • Follow site-specific regulatory and quality standards (e.g., MDSAP, ISO 13485, IVDR) and perform other duties as assigned to support business needs.
Physical Attributes
  • Meet vision standards as outlined by occupational guidelines.
  • Lift and move up to 25 lbs and occasionally push up to 25 lbs unassisted.
  • Frequently required to sit or stand, depending on the process needs.
  • Occasionally required to climb ladders/step ladders, kneel, stoop, or perform tasks involving full body use.
  • Capable of performing repetitive motions with hands, including fine manipulation such as pipetting or typing.
  • Reach with hands and arms, and occasionally lift or stand for extended periods.
  • Perform tasks requiring simultaneous use of multiple physical abilities, as needed by the process.
Who You Are

Minimum Qualifications:

  • Associates Degree in any Life Science discipline.
  • 2+ years of cell culture experience.
Preferred Qualifications
  • Experience following Standard Operating Procedures, accurate completion of Manufacturing.
  • Procedure batch records, and adherence to Quality and Regulatory.
  • Bachelor's Degree in any Life Science discipline.
  • Previous experience in FDA regulated biotechnology or pharmaceutical environment.
  • Knowledge of FDA QSRs and ISO 13485 or other related industry standards.
  • Experience with SAP or other ERP system.
  • Excellent computer skills, including MS 365 as well as organizational skills and attention to detail.
  • Excellent time management and project management skills.
  • Knowledge of SAP NEXT.

Pay Range for this position: $23.00-$42.00 per 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 .

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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Position Requirements
10+ Years work experience
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