Reviewing batch records and quality documents, writing and revising SOPs, conducting internal audits, investigating deviations and CAPAs, supporting regulatory submissions, and maintaining compliance with FDA and ICH guidelines.
Quality Assurance Specialists maintain and improve the quality systems that ensure pharmaceutical and biotech products meet regulatory standards. We find the professionals your organisation needs through dedicated retained search — not job boards.
Speak with a retained recruitment specialist today.
🔒 No hard sell · No obligation · Google Meet
Reviewing batch records and quality documents, writing and revising SOPs, conducting internal audits, investigating deviations and CAPAs, supporting regulatory submissions, and maintaining compliance with FDA and ICH guidelines.
Bachelor's degree in a life science, 2–5 years of cGMP QA experience, and demonstrated knowledge of FDA 21 CFR Parts 210/211 for pharma or 820 for devices. ASQ certification is a meaningful differentiator.
QA professionals with hands-on cGMP and deviation management experience are consistently underestimated in demand. At any given time, multiple pharma organisations are competing for the same small pool of experienced QA specialists.
Ready to start a search for a Quality Assurance Specialist?
📅 Book a Free Consultation25 min · Google Meet · No obligation
Our retained model delivers a pre-screened, credentialled shortlist within 21–40 days. Start with a free, confidential 25-minute consultation.
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