Senior QC Scientist: Stability & Method Reviewer
Biopharma Careers
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Benefits offered by this job
Job summary
Biopharma Careers is seeking a Quality Control Scientific Reviewer in Carlsbad, CA. You will review data from in-process, release, and stability testing and draft/approve technical documents for regulatory readiness. You will lead CAPA generation and collaborate across functions to support GMP documentation and audits.
The role requires 9+ years in GLP/GMP environments and advanced degrees in Chemistry or related Life Sciences, with strong data interpretation and scientific writing skills.
Qualifications
- Bachelor’s Degree in Chemistry, Analytical Science, or related Life Science Discipline.
- 9+ years in GLP/GMP analytical environments in Quality Control or Process and Development.
- Master’s Degree in Chemistry, Analytical Science, or related Life Science Discipline.
- 7+ years in GLP/GMP analytical environments in Quality Control or Process and Development.
Responsibilities
- Provide independent data-driven review across in-process, release, and stability testing.
- Draft, review, and approve technical documents for regulatory readiness.
- Lead CAPA generation and investigations with root-cause analysis.
- Engage cross-functionally on data-driven decisions and regulatory submissions.
Education
Tools
Job description
Biopharma Careers is seeking a Quality Control Scientific Reviewer in Carlsbad, CA. You will review data from in-process, release, and stability testing and draft/approve technical documents for regulatory readiness. You will lead CAPA generation and collaborate across functions to support GMP documentation and audits.
The role requires 9+ years in GLP/GMP environments and advanced degrees in Chemistry or related Life Sciences, with strong data interpretation and scientific writing skills.
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