Scientist III (Quality Control Specialist)
Thermo Fisher Scientific · High Point, NC
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Thermo Fisher Scientific seeks a Scientist III Quality Control Specialist to lead analytical and microbiological quality control activities for pharmaceutical development and manufacturing. The role involves managing test method lifecycles, change controls, specifications, and quality system documentation in support of the Drug Product Division.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Phenom, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Bachelor's degree in Chemistry, Biology, Microbiology, or related physical science
- Minimum 8 years of quality control, analytical testing, or pharmaceutical manufacturing experience
- Strong knowledge of GMP, GLP, data integrity, and controlled documentation systems
- Proficiency with analytical techniques including HPLC, GC, LC/MS, dissolution, and spectroscopy
- Experience with change control, technical transfer, specification management, and risk assessment
- Advanced problem-solving and cross-functional collaboration skills
- Excellent written and verbal communication abilities
What you'll be doing
- Evaluate and approve analytical data; lead quality initiatives and mentor junior team members
- Manage method lifecycle activities including gap assessments, transfer, qualification, and validation
- Assess compendial updates and author revision protocols with associated quality system changes
- Own change controls for test procedures, specifications, and raw material manufacturer changes
- Author and maintain quality documents including protocols, SOPs, specifications, and policy documentation
Privacy & handoff
This role links to Thermo Fisher Scientific's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.