Quality Assurance Specialist

Oncotelic

San Diego, CA

JOB DETAILS
SKILLS
Artificial Intelligence (AI), Biology, Biotech and Pharmaceutical, Change Control, Chemistry, Clinical Practices/Protocols, Clinical Trial, Continuous Improvement, Decision Support, Detail Oriented, Document Management, Documentation, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), GxP, ICH Regulations, Internal Audit, Manufacturing Operations, Quality Assurance, Quality Control, Regulations, Research & Development (R&D), Risk Analysis, Risk Management, Standard Operating Procedures (SOP), Structured Data, Team Player, Vendor/Supplier Evaluation
LOCATION
San Diego, CA
POSTED
Today

AI-Enabled Quality Systems | Biotech / GMP EnvironmentJoin 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 DoOwn 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.What Makes This Role DifferentYou 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.What We're Looking ForBachelor'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, MasterControl, TrackWise, etc.) is a plus.Why Join UsWork 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.#J-18808-Ljbffr

About the Company

O

Oncotelic