jobid=A.0.0566
Quality Control Officer
Location: Breda Area (Hybrid – minimum 24h/week onsite)
Duration: 5 months (temporary assignment)
Start Date: 01 November 2025
Hours: Full-time
About the Role
A globally recognized pharmaceutical company is seeking a detail-oriented and GMP-savvy Quality Control Officer to support its radioligand therapy operations. This is a temporary assignment offering hands-on experience in a highly regulated and innovative environment focused on life-saving treatments.
Position Overview
As Quality Control Officer, you will ensure the accurate execution of quality control processes for medicinal products, intermediates, and raw materials. You’ll work closely with internal teams to manage analytical procedures, environmental monitoring, and deviation investigations, contributing to the continuous improvement of laboratory systems and compliance standards.
Key Responsibilities
- Perform QC testing according to product specifications and analytical methods
- Identify and report deviations or unexpected incidents to the Qualified Person
- Conduct environmental monitoring and trend analysis
- Manage documentation and qualification activities, escalating delays when needed
- Collaborate on validation, revalidation, and technology transfers
- Lead deviation and OOS/OOX investigations
- Support change control, calibration, and SOP generation
- Recommend improvements to lab equipment, software, and methods
- Maintain a clean and safe laboratory environment
- Adhere to radiation and conventional safety regulations
About You
- Bachelor’s degree in chemistry, biochemistry, microbiology, or related life sciences
- 1+ year of experience in pharmaceutical QC within a regulated environment
- Strong knowledge of cGMP and good laboratory practices
- Analytical mindset with attention to detail
- Proactive, collaborative, and open to new technologies
- Fluent in English, Dutch is a pre (spoken and written)
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