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At Capgemini Engineering, you will contribute to the technical execution of pharmaceutical projects as part of the Engineering Process department.
Your Role
- Install and integrate new pharmaceutical equipment.
- Design modifications of existing equipment.
- Prepare technical documentation such as URS, FS, and DS.
- Manage suppliers and execute Factory Acceptance Tests (FAT).
- Support IQ, OQ, and PPQ phases.
- Draft FAT, Design Review, and Commissioning protocols.
- Track and close punch lists from FAT and commissioning activities.
- Participate actively in C&Q project governance and execution.
You will initially work closely with a Process Engineering Subject Matter Expert and progressively take ownership of defined commissioning and C&Q activities.
Your Profile
- Rapidly absorb additional C&Q-related responsibilities.
- Develop toward autonomy on smaller-scale projects.
- Hold an engineering degree or a Master’s degree in Applied Sciences; extensive relevant experience may compensate, while a Bachelor’s degree alone is insufficient.
- Have proven experience in a pharmaceutical or biopharmaceutical GMP environment.
- Experience with fill and finish equipment or process setup equipment is a strong asset.
- Have practical experience with FAT, commissioning, IQ/OQ, and supplier interactions.
- Bring a pragmatic, field-oriented engineering approach and the ability to work on-site.
- Be fluent in French and English.
- Be mobile to Lessines.
What You Will Love About Working Here
- Communities that support career development through the Engineering Career Framework.
- Tech for Societal Solutions initiatives addressing humanitarian, health, and biodiversity challenges.
- Career acceleration programs supporting development at every stage.
Capgemini is a global business and technology transformation partner with 340,000 team members in more than 50 countries.