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QC Specialist II

Katalyst Healthcares and Life Sciences

Job Description:
The Quality Control Technical Transfer Analyst 3 supports the QC department by performing analytical testing, assisting with technical transfer activities, and maintaining quality documentation in a GMP-regulated pharmaceutical or biotechnology environment. The role involves executing laboratory testing, reviewing data, supporting validations and investigations, and ensuring compliance with GMP and Data Integrity requirements.

Roles and Responsibilities:

  • Perform analytical testing for in-process samples, lot release, and stability studies.
  • Support technical transfers, method validations, and laboratory investigations.
  • Review analytical data and ensure results meet quality and compliance standards.
  • Prepare and maintain quality documentation such as Deviations, CAPA, Change Control, and Investigations.
  • Use laboratory systems and software including SoftmaxPro, Empower, SoloVPE, LIMS, and TrackWise.
  • Support software validation activities, including writing procedures and executing validation test scripts.
  • pply GMP and Data Integrity principles in all laboratory activities.
  • Collaborate with cross-functional teams and provide training when required.
  • Perform root cause analysis for laboratory or software-related issues.
Requirements:
  • 3-5 years of experience in a Quality Control laboratory within the pharmaceutical or biotechnology industry.
  • Experience working in a GMP-regulated environment.
  • Hands-on experience with analytical testing, method transfers, validations, and investigations.
  • Experience with quality systems such as Deviations, CAPA, Change Control, and LIMS/TrackWise is preferred.
  • ssociate's Degree in Microbiology, Biochemistry, Biotechnology, Chemistry, or a related Life Sciences field.
Vacancy posted 1 day ago
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