Engineer Product Support – Stability | Brussels

Prothya Biosolutions; Brussel Hoofdstad; Hybride; EUR 50 000 - 70 000; Plein temps

Avantages offerts par ce poste

Growth opportunities

Competitive salary

Insurance

Meal vouchers

Eco-cheques

Flex Reward Plan

Extra holidays

Hybrid work after onboarding

Résumé du poste

Prothya Biosolutions in Brussels is seeking a Product Support Engineer to enhance their QC Support Global team with a focus on stability studies. This role involves managing stability planning, protocols, and fostering collaborations across departments.

The ideal candidate will hold a Master’s degree in Engineering, Biotechnology, or Biochemistry, possess 3+ years in a GMP-driven environment, and be fluent in English alongside Dutch or French. The position offers growth within an international biopharma group and a supportive work environment.

Qualifications

• Master’s degree in Engineering, Biotechnology, or Biochemistry.
• 3+ years of experience in a GMP-driven environment.
• Strong understanding of ICH & EudraLex GMP stability requirements.

Responsabilités

• Manage stability planning and protocol creation.
• Follow up QC testing, raw data, and reporting.
• Collaborate with multiple departments and support audits as Stability SME.

Connaissances

GMP knowledge

Analytical skills

Organizational skills

Communication skills

Team-oriented

Fluency in English

Fluency in Dutch or French

Formation

Master's degree in Engineering, Biotechnology, Biochemistry

Description du poste

Product Support Engineer – Stability (Prothya Biosolutions Belgium)

Prothya Biosolutions develops plasma‑derived medicines that improve the lives of millions of patients. To support this mission, we’re looking for an Engineer to strengthen our QC Support Global team with a focus on stability studies.

Your responsibilities

• Manage stability planning and protocol creation
• Follow up QC testing, raw data, and reporting
• Maintain SOPs and align with our NL site
• Handle investigations and Quality Management System records
• Collaborate with multiple departments and support audits as Stability SME
• Contribute to improvement projects within the team

Your profile

• Master’s degree in Engineering, Biotechnology, Biochemistry…
• 3+ years’ experience in a GMP‑driven environment
• Strong understanding of ICH & EudraLex GMP stability requirements
• Analytical, organized, communicative, and team‑oriented
• Fluent in English + Dutch or French

What we offer

• Growth opportunities within an international biopharma group
• Competitive salary, insurance, meal vouchers, eco‑cheques
• Flex Reward Plan
• Extra holidays
• Hybrid work after onboarding
• A respectful, diverse, and supportive environment

If you’re looking for a role with impact and room to grow, we’d be happy to meet you.