QC Specialist 2

Katalyst HealthCares and Life Sciences

Posted on: July 16, 2026

Closing: August 15, 2026

Salary: Undisclosed

Job Description

Job Description:
The QC Technical Transfer Analyst 3 supports the Quality Control department by performing analytical testing, executing technical transfer activities, and maintaining GMP-compliant documentation. The role involves semi-routine testing, data interpretation, software system usage, and participation in investigations, method transfers, and validation projects. The analyst must be able to recognize deviations, solve moderate-scope problems, and communicate effectively with cross-functional teams.
Responsibilities:
  • Perform QC testing for In-Process, Lot Release, Stability, investigations, transfers, and validations.
  • Review assays and ensure compliance with GMP, Data Integrity, and Lonza policies.
  • Write and manage Quality Records: Deviations, CAPA, Change Control, EICRs, Investigations, Test Methods.
  • Support method transfers, new instrument onboarding, and method qualifications.
  • Train team members on QC processes and laboratory systems.
  • Use QC software systems: SoftmaxPro, Empower, SoloVPE, TrackWise, LIMS, Microsoft Office Suite.
  • Execute software validation tasks: writing GMP procedures, validation documents, test scripts.
  • ct as SME for at least one QC software system.
  • Perform root-cause analysis for software-related issues.
  • pply Data Integrity principles in all work activities.
  • Communicate with cross-functional teams to understand priorities and project needs.
  • Complete assigned tasks accurately and on time; maintain positive team communication.
  • Follow all assigned training and maintain compliance with GMP requirements.
  • Perform other duties as assigned.

Requirements:
  • ssociate's Degree in Microbiology, Biochemistry, Biotechnology, Chemistry, or related scientific field.
  • 3-5 years experience in Quality Control within a GMP pharmaceutical or biotech environment.
  • Hands-on experience with:

o Change Control, Deviations, CAPA, Investigations

o QC testing (release, stability, in-process)

o Laboratory software systems (SoftmaxPro, Empower, SoloVPE)

o GMP documentation and software validation.
  • bility to interpret data, solve moderate-scope problems, and communicate clearly.
  • Experience working in cross-functional teams and supporting technical transfer projects.

Katalyst HealthCares and Life Sciences

Posted on: July 16, 2026

Closing: August 15, 2026

Salary: Undisclosed

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