Scientist I, Microbiology

ProBio•Pennington, NJ
•$70,000 - $83,000

About The Position

The position reports to the Manager of Microbiology, is ideally suited for a professional with technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to learn this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients.

Requirements

  • Bachelor’s degree in, Microbiology, Biology, Biochemistry or related scientific field with 2-5 years of relevant work experience.
  • Familiar with principles of Good Documentation Practices, Data Integrity, ALCOA+
  • Experience following Standard Operating Procedures or protocols.
  • Ability to problem solve, and work independently and as part of a team.
  • Experience with Microsoft Office tools.
  • Strong interpersonal, verbal, and written communication skills

Responsibilities

  • Sample Collection and Processing: Environmental Monitoring of cleanrooms, Water Testing, and Gas Testing.
  • Support QC-Microbiology laboratory procedures: development and updating of governing procedures and methods.
  • Support QC-Microbiology Product testing: routine testing on products, verification testing on products, method suitability, training, development, updating of governing procedures and methods for product testing.
  • Support QC-Microbiology media fills: monitoring and testing of media fills.
  • Microorganism Analysis: Not limited to, activities such as Plate Reads, Gram Staining, Growth Promotion, Bioburden, Endotoxin, Gowning Qualifications, mycoplasma, plasmid retention, Biological indicators, aseptic training, and other QC-Microbiology activities.
  • Participate in EMPQ, cleanroom validation, and associated activities/documents.
  • Responsible for following cGMP in carrying out functions related to QC testing.
  • Support optimization initiatives to improve QC department, such as lab inventory, sample workflow, and lab preparation.
  • Perform other duties, as assigned based on business needs.

Benefits

  • medical, dental, and vision insurance
  • 401(k) retirement plan with a company match that vests fully on day one
  • paid parental leave after just three (3) months of employment
  • paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays
  • flexible spending and health savings accounts
  • life and AD&D insurance
  • short- and long-term disability coverage
  • legal assistance
  • supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance
  • commuter benefits
  • well-being initiatives
  • peer-to-peer recognition programs
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