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Bioengineering Process Scientist (Biologics )

LocationBrussels , Belgium
Business SectorBiotechnology
Contact email
Job ref26794
Published39 minutes ago

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