Senior QA Associate — Clinical Manufacturing & Supply Chain

People in Science; Breda; On-site; EUR 60,000 - 80,000; Full time

Job summary

People in Science in Breda seeks a Senior Associate Quality Assurance to provide QA oversight of both clinical manufacturing and clinical supply chain activities. You will support labelling, packaging, and documentation reviews while ensuring GMP/GDP compliance and coordinating with Production, Warehouse, Supply Chain and Regulatory Affairs.

Ideal candidates have a Life Sciences degree (Master’s preferred) and 1–3 years of GMP-regulated QA experience, with strong analytical and communication

Qualifications

• Degree in Life Sciences, Pharmaceutical Sciences, Biotechnology or related field (Master’s preferred).
• 1–3 years QA experience in GMP-regulated environment; more for senior candidate.
• Experience in pharma/medical device industry preferred.
• Knowledge of GMP, GDP and/or GCP regulations.
• Experience with batch record reviews, deviations, investigations, or similar QA activities.
• Strong analytical skills and attention to detail.
• Good communication and cross-functional collaboration.
• Fluency in English.

Responsibilities

• Provide QA oversight of clinical manufacturing and clinical supply chain activities.
• Perform QA on the production floor and document reviews.
• Review and approve deviations, ensuring GMP compliance.
• Support labeling and packaging with GMP/GDP compliance.
• Prepare monthly quality metrics and identify improvements.
• Collaborate with Production, Warehouse, Supply Chain, QA and Regulatory Affairs.
• Write, review and update SOPs and Work Instructions.

Skills

Quality mindset

Analytical thinking

Communication skills

Teamwork

Fluency in English

Education

Life Sciences degree

Master's degree preferred

Job description

People in Science in Breda seeks a Senior Associate Quality Assurance to provide QA oversight of both clinical manufacturing and clinical supply chain activities. You will support labelling, packaging, and documentation reviews while ensuring GMP/GDP compliance and coordinating with Production, Warehouse, Supply Chain and Regulatory Affairs.

Ideal candidates have a Life Sciences degree (Master’s preferred) and 1–3 years of GMP-regulated QA experience, with strong analytical and communication