Senior QA Specialist - cGMP, QMS & Audit Readiness

Vivid Resourcing Ltd; Limburg; In loco; EUR 83.000 - 117.000; Tempo pieno

Descrizione del lavoro

Vivid Resourcing Ltd is working with a client in Limburg to appoint a Senior QA Specialist with a strong pharmaceutical quality background to support the Lead Qualified Person (QP) and ensure batches are manufactured and tested in compliance.

The role covers QMS improvement, CAPA, deviations, change control, batch documentation, and audits. Fluent Dutch is required; expected start October/ASAP; 40 hours per week; freelance contract.

Competenze

• Master's degree or equivalent in a related field with pharmaceutical manufacturing experience.
• 3–5 years of QA experience in pharma or food manufacturing.
• Strong knowledge of international cGMP guidelines and regulations.
• Experience with (secondary) pharmaceutical packaging processes is an asset.

Mansioni

• Maintain and improve the Quality System to meet cGMP standards.
• Support QP and review batch documentation and deviations.
• Lead or support CAPA, investigations, and change controls.
• Prepare APR/PQR and participate in audits.
• Provide training and cross-functional project support.

Conoscenze

Detail-oriented

Team player

Ownership

Integrity

Organized

Formazione

Master's degree in Industrial Pharmacy

Biomedical Sciences / Bioengineering equivalent

Descrizione del lavoro

Vivid Resourcing Ltd is working with a client in Limburg to appoint a Senior QA Specialist with a strong pharmaceutical quality background to support the Lead Qualified Person (QP) and ensure batches are manufactured and tested in compliance.

The role covers QMS improvement, CAPA, deviations, change control, batch documentation, and audits. Fluent Dutch is required; expected start October/ASAP; 40 hours per week; freelance contract.