QC Specialist 2
Portsmouth, New Hampshire, United States
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:
Requirements:
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.
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.
Apply
This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.