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Senior Analytical MSAT / QC Validation Consultant Liège, Belgium – 3-month contract (extension likely) Job Description You will join a biopharma/ATMP manufacturing environment, supporting MSAT, PAD, and QC activities with senior-level analytical and validation expertise. The role exists to ensure robust qualification and validation strategies, compliant GMP documentation, and sustained analytical method performance across the analytical lifecycle. This position has a strong strategic and hands-on advisory focus, acting as an SME across MSAT and QC while interfacing with internal teams, clients, and auditors. You will play a key role in method lifecycle governance, validation strategy, and audit readiness in a fast-paced GMP setting. Essential Requirements MSc or PhD in Analytical Chemistry, Pharmaceutical Sciences, Biotechnology, or related discipline Minimum 5+ years’ experience in Analytical Validation / Qualification & Validation Strong background in GMP analytical method lifecycle (MSAT, PAD, QC) Proven experience defining and executing validation and qualification strategies Strong knowledge of FDA and EU GMP regulations Ability to act independently at senior advisory / SME level Excellent scientific writing, documentation review, and approval capabilities Preferred Requirements Experience in biopharmaceutical and/or ATMP environments Exposure to method transfer (client-derived and internal PAD/QC transfers) Familiarity with Total Error approach and statistical assessment of validation data Experience supporting regulatory and client audits Ability to coach and support MSAT experts and Q&V technicians French language skills Practicalities Start Date: ASAP (immediate availability preferred) Contract Duration: 3 months (extension highly likely) Location: Hybrid Additional: High-urgency assignment; fast decision-making process Interested? Interviews and offers can move quickly. Send your CV to Katelijne or reach out directly to discuss availability and fit.