GMP Validation Specialist - Onsite Antwerp (Freelance)

Vivid Resourcing; Antwerpen; On-site; EUR 69,000 - 96,000; Full time

Job summary

Vivid Resourcing is seeking a freelance QA Validation Officer in Antwerp for a hands-on role focused on validating protocols and ensuring compliance with GMP requirements. You will prepare and execute validation activities, maintain documentation, and support CAPAs and change controls across QA, Engineering, and Production teams.

The role requires strong technical writing, attention to detail and ability to work independently in a cross-functional environment.

Qualifications

• Minimum 3 years of experience in validation, qualification or QA within a GMP-regulated pharmaceutical or biotechnology environment.
• Proven hands-on experience writing and executing validation protocols.
• Strong knowledge of GMP regulations and validation lifecycle principles.

Responsibilities

• Write, review and execute validation and qualification protocols, including IQ, OQ and PQ.
• Prepare validation documentation, including Validation Plans, URS, Risk Assessments and Validation Reports.
• Support qualification and validation of manufacturing equipment, processes, utilities and systems.
• Ensure validation activities are performed in compliance with EU GMP, Annex 15 and internal procedures.
• Execute validation testing on-site with accurate documentation and full traceability.
• Identify, document and investigate deviations arising during protocol execution.
• Support CAPAs, change controls and validation-related quality events.
• Review executed protocols and compile final validation reports.
• Collaborate with QA, Engineering, Production and Validation teams to ensure timely completion.
• Maintain inspection-ready GMP documentation.
• Support continuous improvement initiatives related to validation procedures and quality compliance.

Skills

Validation

GMP

Documentation

IQ/OQ/PQ

Quality Assurance

Job description

Vivid Resourcing is seeking a freelance QA Validation Officer in Antwerp for a hands-on role focused on validating protocols and ensuring compliance with GMP requirements. You will prepare and execute validation activities, maintain documentation, and support CAPAs and change controls across QA, Engineering, and Production teams.

The role requires strong technical writing, attention to detail and ability to work independently in a cross-functional environment.