Quality Assurance Associate (Pharmaceutical – 3-Shift Role) Breda • SIRE Life Sciences

Quality Assurance Associate (Pharmaceutical – 3-Shift Role)
Location: Breda
Schedule: Rotating Shifts (Early, Late, Night)

• Provide on-the-floor QA support during pharmaceutical packaging and labeling operations
• Perform in-process product checks and GMP compliance monitoring
• Review and approve batch record data entries before and after production
• Act as a first point of contact for quality-related questions in production
• Support investigations, deviations, and change control activities
• Assist in writing and reviewing Standard Operating Procedures (SOPs) and Work Instructions
• Participate in quality improvement initiatives and GMP training efforts
• Contribute to weekly/monthly quality metrics and team performance tracking

• MBO, HBO, or BSc degree in Life Sciences, Pharmaceutical Technology, Biotechnology, Chemistry, or related fields
• A strong interest in working in GMP-compliant pharmaceutical environments
• Excellent communication skills and a proactive, collaborative mindset
• Comfortable working in a 3-shift structure
• Previous experience in a GMP production or lab setting is a plus — but not required
• Fluent in English (written and spoken); Dutch is a plus

• Working in a leading international biotech organization
• Hands-on training and ongoing development in Quality Assurance
• A chance to work with experienced QA professionals in a collaborative, supportive team
• Competitive salary and shift allowances
• A meaningful career helping bring critical medicines to patients worldwide

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