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@ Catalent
  • Post Date : Jun 26, 2025
  • Apply Before : Jul 26, 2025
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Job Detail

  • Offered Salary 0
  • Commitment Full Time
  • Compensation Paid
  • Required education level Bachelor’s degree

Job Description

The Role:

  • Manage and maintain client samples, ensuring proper storage and inventory tracking
  • Draft and finalize stability protocols and reports (interim and final)
  • Perform stability timepoint pulls and aliquot samples according to established protocols and timelines.
  • Coordinate and submit samples to internal and external laboratories for testing
  • Oversee stability studies, ensuring samples are tested and reported within the allotted windows
  • Maintain accurate records and documentation in accordance with Good Documentation Practices (GDP)
  • Assist in troubleshooting and resolving issues related to stability studies
  • Other duties as assigned.

The Candidate:

  • Degree in Biology, Life Science or Chemical Engineering field (A.S. with 1-3 years’, or B.S. with < 1 year of experience)
  • The ability to work in team-oriented environment is essential, as this person will work closely with other members of Analytical Development, Process Development, QC, and Operations.
  • Previous experience working in Biotechnology or Pharmaceutical industry considered a plus
  • The position involves regularly sitting at a desk and working on a computer, standing, and walking for extended periods Must be able to lift to 15 pounds at times. The role requires the use of both laboratory and office equipment, with office-related tasks performed in a shared office space adjacent to the lab.

Apply Now Application ends in 27d 19h 7min
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