Validation Engineer

Validation Engineer

Contracting - Wavre

Your Responsibilities

As a Validation Coordinator, you will play a key role in supporting validation activities for live viral vaccine bulk production in a GMP environment. Your main tasks include:

• Coordinate and execute validation activities on the shopfloor related to cleaning (UF, WAM, transfer lines) and sterility assurance
• Deliver continuous validation and support for eCC (engineering Change Control) and project validation for the Manufacturing Unit (MU - LVV)
• Author, review, and approve validation documentation, including IQ/OQ/PQ protocols, rationales, checklists, and validation deviations
• Support impact assessments and risk analyses (e.g. bioburden/endotoxin risk, APS, EM qualification, etc.)
• Ensure alignment with internal QA standards and participate in cross-functional coordination with production, QA, and engineering teams
• Act as validation subject matter expert (SME) during audits or inspections when required

Your Profile

• Minimum 2 years of experience in a pharmaceutical manufacturing or QA/validation role
• Experience in cleaning validation and sterility assurance is required
• Strong understanding of validation documentation and GMP compliance
• Ability to manage priorities and coordinate cross-functional stakeholders
• Excellent communication and problem-solving skills
• Fluent in English (French is a plus)

Our offer:

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You're interested in this job? We kindly invite you to apply or send me your CV,