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Quality Assurance Specialist
Job in
San Diego, San Diego County, California, 92189, USA
Listed on 2026-01-27
Listing for:
Oncotelic
Full Time
position Listed on 2026-01-27
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
Job Description & How to Apply Below
AI-Enabled Quality Systems | Biotech / GMP Environment
Join a next-generation biotech organization redefining Quality Assurance through AI-enabled knowledge systems.
We are seeking a QA Specialist to support and strengthen our GxP quality framework while leveraging PDAOAI, our proprietary AI platform that transforms static SOP libraries into functional, queryable, decision-support systems.
What You’ll Do- Own and maintain GMP / GxP SOPs, policies, and controlled documents across QA, QC, Manufacturing, and Clinical operations.
- Use PDAOAI to interrogate and cross‑reference SOPs, deviations, CAPAs, and training records.
- Identify inconsistencies, gaps, and misalignment across the SOP corpus.
- Translate regulatory guidance into actionable, harmonized procedures.
- Support deviation investigations, CAPAs, change controls, and risk assessments.
- Participate in internal audits, vendor audits, and regulatory inspections.
- Ensure SOPs are not just compliant but operationally executable and inspection‑ready.
- Collaborate cross‑functionally with CMC, Clinical, Regulatory, and Operations teams.
- You will not be maintaining static PDFs.
- You will functionalize the SOP corpus—turning procedures into living, AI‑assisted quality assets.
- You will help define how AI augments QA decision‑making, inspection readiness, and continuous improvement.
- You will work in a culture where Quality is strategic, not administrative.
- Bachelor’s degree in Life Sciences, Chemistry, Engineering, or related field.
- 3+ years of QA experience in a GMP / GxP‑regulated environment (biotech, pharma, CDMO, or clinical trials).
- Strong working knowledge of SOP lifecycle management; deviations, CAPAs, change control; FDA, EMA, ICH, and Annex 1 expectations (as applicable); comfort working with digital systems, structured data, and AI‑assisted tools.
- Detail‑oriented, systems‑thinking mindset with strong documentation skills.
- Prior experience with QMS platforms (Veeva, Master Control, Track Wise, etc.) is a plus.
- Work with a cutting‑edge AI platform (PDAOAI) purpose‑built for regulated environments.
- Influence how Quality evolves in the age of AI.
- High‑impact role with visibility across R&D, CMC, and Clinical programs.
- Collaborative, science‑driven culture with strong executive engagement.
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