CareerPlan

Analytical Method Validation Specialist

Wavre, Wallonia, beFull-time2026-10-05 → 2026-11-10
Based in Belgium

Core

Coordinate and implement analytical method validation activities to support Quality Control operations in a pharmaceutical setting, ensuring compliance with GMP requirements.

Role type

Analytical Method Validation Specialist

Builds

Validated analytical methods for pharmaceutical quality control

Domain

Pharmaceutical industry, Quality Control, Analytical Chemistry

Required skills

Analytical method validation, GMP compliance, Technical documentation writing, Change control management, Deviation management, CAPA management, Risk-based decision making

Preferred skills

None stated

Technologies

None stated

Responsibilities

Write and maintain validation documentation (protocols, reports, amendments, risk assessments), Coordinate multi-stakeholder validation projects, Support quality systems processes (deviations, change controls, CAPAs), Participate in peer reviews and quality audits, Identify opportunities for process improvement

Seniority

Mid-level, hands-on IC