Role Description
We are seeking a highly specialized Bioengineering Process Scientist to support biologics and gene therapy programs within a leading global biopharmaceutical organization.
This role operates at the interface of development and manufacturing, supporting clinical supply (Phase I–III) and ensuring robust process performance within a GMP-regulated environment. The position requires strong bioengineering expertise combined with in-depth process knowledge in biologics manufacturing.
The successful candidate will play a key role in managing deviations, change control, CAPA activities, and supporting process scale-up and technology transfer initiatives.
Sector:
Biologics & Gene Therapy Manufacturing
Non-Negotiable Skills and Experience (Must-Haves)
- BSc or MSc in Biotechnology, Biochemistry, Bioengineering, or related field
- Minimum 5 years of relevant experience in biologics or gene therapy manufacturing
- Proven hands-on experience in biologics manufacturing within a GMP-regulated environment as well as process scale-up, and technology transfer
- Demonstrated experience managing deviations, investigations, change control, and CAPA processes
- Experience supporting clinical studies (Phase I–III) from a manufacturing/process perspective
- Professional working proficiency in English
Essential Skills and Experience (Should-Haves)
- Experience operating across both development (clinical supply) and commercial manufacturing environments
- Strong cross-functional collaboration skills (Quality, Manufacturing, Engineering, Regulatory)
- Experience in process troubleshooting and continuous improvement initiatives
- Good understanding of GMP documentation and regulatory expectations
- Strong analytical and problem-solving mindset
Desirable Skills and Experience (Nice-to-Haves)
- Experience in gene therapy programs specifically
- Experience supporting late-stage clinical manufacturing
- Familiarity with regulatory submissions or inspection readiness activities
- French language skills (asset for local collaboration)
Practicalities
Location: Wallonia region, Belgium (Braine-l’Alleud area preferred)
Duration: 12 months (contract, with possible extension)
Start Date: 1 April 2026
Work type: On-site
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