MSAT Quality Engineer | Life Science

Your Role

We are looking for an experienced Pharma MSAT Quality Lead to join our team in Brussels. In this senior, autonomous role, you will provide expert QA support across multiple pharmaceutical projects, acting as a trusted quality partner across technology transfers, process validation, and cross-functional initiatives. You will play a pivotal role in ensuring that our clients' products and processes meet the highest regulatory and quality standards.

In this role you will play a key role in:

• Supporting technology transfers across Drug Substance, Drug Product, and Packaging — providing hands-on QA expertise throughout process and analytical transfer activities
• Acting as second-line support for complex or cross-site quality issues, leading investigations, managing deviations, and driving robust CAPA definition and follow-up
• Ensuring quality oversight during process validation and Continuous Process Verification (CPV), contributing to both project-based and transversal quality activities
• Participating in cross-functional governance and project meetings, monitoring timelines, risks, and deliverables while providing expert QA input on complex technical topics
• Reinforcing quality teams during peak periods, including support for quality agreements and vendor QA activities, ensuring continuity and compliance across all initiatives

Your profile

We are looking for a senior quality professional who brings both technical depth and the ability to work autonomously in complex, international environments.

• You bring a minimum of 5 years of experience in pharmaceutical quality, with a strong operational QA background and the ability to understand, challenge, and contribute to technical content
• You have proven experience managing complex investigations, deviations, and CAPA processes within a regulated pharmaceutical environment, with a solid understanding of GMP and applicable regulatory frameworks
• You have hands-on experience in technology transfer (process and/or analytical), ideally in a QA context, across one or more of Drug Substance, Drug Product, or Packaging
• You are an excellent communicator in English (written and verbal), comfortable operating across cross-functional and international teams, and capable of engaging confidently with diverse stakeholders
• Experience in biologics, exposure to multicultural or global teams, and French language skills are considered strong assets

What you'll love about working here

Inclusive leadership – Capgemini collaborates with global organizations to strengthen an equal opportunities framework, including promotion and pay, and to empower our leaders to develop inclusive behaviors and combat bias (97% of our VPs went through training on unconscious biases).

Tech for Societal Solutions – We're committed to addressing emerging crises, be it humanitarian, health, or biodiversity, to the best of our abilities. Collaborating with projects like ITER to build a safer, large-scale source of energy, our global scientists and experts work every day to make the world a better place.

Continuous feedback – We take a human-centric approach to foster growth and performance. Our performance management tool GetSuccess enables continuous feedback, quarterly check-ins with managers, and ongoing performance discussions.