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QA Specialist

Le Trait, FR💼 Full-time💰 $42,400–$42,400🗓 2026-09-28

Core

On-site Quality Assurance Specialist ensuring production compliance with regulatory requirements and GMP standards, resolving quality issues in real-time, and managing deviations and CAPAs.

Role type

Senior IC Quality Assurance Specialist (Pharmaceutical Manufacturing)

Builds

Pharmaceutical products and vaccines

Domain

Pharmaceutical manufacturing / Regulatory compliance

Required skills

GMP compliance, deviation management, CAPA strategy, root cause analysis, audit execution, performance indicator monitoring, aseptic environment knowledge

Preferred skills

Microbiology knowledge, experience in aseptic environments

Technologies

GMP systems, deviation management systems

Responsibilities

Ensure production activities comply with regulatory requirements and GMP; Collaborate with production teams to maintain quality standards; Manage and resolve quality issues within deadlines; Handle deviations, approvals, and CAPA strategies; Monitor and analyze quality performance indicators; Conduct regular production process audits; Participate in internal, external, and regulatory inspections.

Seniority

Mid-Senior, hands-on IC

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