Process Validation Engineer CAR-T; F​/H​/X

Permanent Job

As a Process Validation Engineer, Cell Therapy
, you’ll join the Manufacturing Excellence team supporting the start-up of a new CAR-T production site in Ghent.

You’ll contribute to the implementation of the pilot plant and the launch of the CAR-T manufacturing process, with a focus on tech transfer, process and sterilization validation, equipment introduction, and technical documentation.

Working with cross-functional teams, you’ll help ensure that manufacturing activities are ready for compliant and reliable production.

• Define, plan, and coordinate validation activities for the CAR-T pilot plant in Ghent, including PPQ, smoke studies, hold time validation, APQ, and APS.
• Provide technical guidance on process validation and equipment qualification activities.
• Lead the revalidation of manufacturing and sterilization processes.
• Write, review, and approve validation strategies, plans, protocols, reports, and related technical documentation.
• Support tech transfer, product introduction, equipment implementation, and system introduction activities.
• Review technical reports and procedures to ensure compliance with cGMP, regulatory requirements, and current industry practices.
• Contribute to process improvement projects, while tracking activities, risks, and deliverables with project teams and leadership.

• Bachelor’s degree or higher in Engineering, Biotechnology, Biomedical Sciences, Pharmacy, or a related field.
• Experience in pharmaceutical, biotechnology, cell therapy, human plasma-derived products, or a comparable regulated industry.
• Experience introducing pharmaceutical products into manufacturing sites, with a good understanding of manufacturing unit operations.
• Strong knowledge of current Good Manufacturing Practices and validation principles.
• Experience working in a controlled cleanroom environment under aseptic conditions is a plus.
• Strong project management, reporting, problem-solving, prioritisation, and decision‑making skills.
• Ability to work independently and as part of a team, communicate with stakeholders at different levels, and work fluently in written and spoken Dutch and English.

Joining Amaris means working in an environment where your performance supports your career progression.

Projects with substance
Our projects last 18 months on average and involve major accounts such as Orange, Sanofi, SNCF, and CMA-CGM. You’ll work on assignments where your experience has a direct impact on project delivery and product quality.

Support from your manager and HR
Each manager supports up to 18 consultants. You’ll have regular project check‑ins and a direct exchange with HR every month through Express Yourself. Our teams have an average tenure of 3.3 years.

Career progression
70% of our managers started in entry‑level positions. Career development is based on skills, performance, and the opportunities you take. Functional mobility across 4 areas of expertise and international mobility across 60+ countries are actively encouraged.

Learning and technology
You’ll have access 250+ training modules, fully funded Microsoft certifications, and 291 AI agents developed in‑house. We support continuous learning throughout your career.

Social and environmental commitments
Our commitment s include an SBTi carbon reduction roadmap, a target of 34.3% women in management by 2029, and social engagement through We Care Together.

• Health insurance, remote work, meal vouchers, a time savings account, and a referral bonus are also available.

We’ll discuss the full benefits package during the recruitment process.

Amaris Consulting is proud to be an equal‑opportunity workplace. We’re committed to building a diverse and inclusive working…