Remote Upstream Bioprocess Engineer for GMP Startup

Capgemini Engineering; Diegem; Hybride; EUR 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

Flexible working arrangements

Résumé du poste

Capgemini Engineering in Belgium is seeking an Upstream Process Engineer to support startup and readiness of a new biotechnologies manufacturing environment. You will collaborate with engineering, manufacturing, validation, and quality teams to drive process excellence.

You bring hands-on experience in upstream processing, bioprocessing, and regulated environments, with strong technical writing and cross-functional communication skills.

Qualifications

• Experience in Upstream Processing, Bioprocess Engineering, or Biomanufacturing.
• Engineering degree or scientific Master’s degree.
• Good understanding of cell culture processes and manufacturing operations.
• Experience working in regulated environments.
• Strong technical writing skills and experience drafting procedures or process documentation.

Responsabilités

• Supporting equipment qualification and commissioning activities from a process perspective.
• Acting as the technical point of contact for upstream manufacturing processes.
• Collaborating with engineering, validation, and operations teams to resolve technical issues.
• Writing and reviewing process documentation, SOPs, risk assessments, and GMP-related procedures.
• Ensuring documentation is practical, clear, and aligned with manufacturing needs.
• Contributing to operational and GMP readiness activities.
• Supporting engineering runs and manufacturing campaign preparation.
• Working closely with cross-functional stakeholders to ensure a smooth transition into routine operations.

Connaissances

Upstream Processing experience

Bioprocess Engineering

Technical writing

Cross-functional communication

French and English fluency

Formation

Engineering degree or scientific Master's degree

Description du poste

Capgemini Engineering in Belgium is seeking an Upstream Process Engineer to support startup and readiness of a new biotechnologies manufacturing environment. You will collaborate with engineering, manufacturing, validation, and quality teams to drive process excellence.

You bring hands-on experience in upstream processing, bioprocessing, and regulated environments, with strong technical writing and cross-functional communication skills.