Quality Control Analyst | Brussels

Prothya Biosolutions; Neder-Over-Heembeek; Sur place; EUR 42 000 - 60 000; Plein temps

Avantages offerts par ce poste

Dynamic company

Learning opportunities

Competitive salary

People-focused culture

Résumé du poste

Prothya Biosolutions Belgium is seeking a Quality Control Analyst to perform QC testing of raw materials and production-related samples in a GMP-regulated environment. You will review analytical results, support OOS/OOT investigations, and ensure GMP-compliant documentation.

With a bachelor’s degree in a related field and at least 3 years in a pharma QC lab, you’ll contribute to method validation, data integrity, and continuous improvement while collaborating across the QC team.

Qualifications

• Bachelor's degree in a related life science field.
• Minimum 3 years of experience in a pharmaceutical QC laboratory.
• Solid understanding of GMP requirements and quality systems.
• Fluency in English with proficiency in French or Dutch.

Responsabilités

• Perform QC testing of raw materials and production-related samples.
• Review analytical results and support OOS/OOT investigations.
• Ensure GMP-compliant documentation and data integrity (ALCOA+).
• Contribute to method validation, qualification, and continuous improvement.
• Provide technical support within the QC team.

Connaissances

Quality control

GMP compliance

OOS/OOT investigations

ALCOA+

Formation

Bachelor's degree in Biochemistry Biotechnology Microbiology Industrial Pharmacy or related field

Description du poste

We're Hiring: Quality Control Analyst | Prothya Biosolutions Belgium

Are you passionate about Quality Control in a GMP-regulated environment? Join Prothya Biosolutions and help deliver life-saving plasma-derived medicines to millions of patients worldwide.

Your Responsibilities

• Perform quality control testing of raw materials and production-related samples
• Review and interpret analytical results and support OOS/OOT investigations
• Ensure accurate GMP-compliant documentation and data integrity (ALCOA+)
• Contribute to method validation, qualification, and continuous improvement projects
• Provide technical support and share expertise within the QC team

Your Profile

• Bachelor's degree in Biochemistry, Biotechnology, Microbiology, Industrial Pharmacy, or a related field
• Minimum 3 years of experience in a pharmaceutical QC laboratory
• Solid understanding of GMP requirements and quality systems
• Good command of English and proficiency in French or Dutch
• Strong analytical mindset, attention to detail, and problem-solving skills

What We Offer

• A dynamic and growing international biopharmaceutical company
• Continuous learning and development opportunities
• Competitive salary package with attractive benefits and Flex Reward Plan
• A collaborative, innovative, and people-focused work environment

Ready to make a difference in patients’ lives? Apply now or share this opportunity with your network!