Quality Specialist Operations
Contracting – Anvers
Your Responsibilities:
- Investigate and document QA-related deviations, escalating issues or providing recommendations to the Team Leader as needed
- Coordinate cross-functional investigations involving manufacturing, packaging, labs, support teams, and third parties
- Perform root cause analyses, define CAPAs, and verify their effectiveness to prevent recurrence
- Report significant quality events to regulatory agencies (e.g., FAR, BPDR) in compliance with local and international regulations
- Participate in operational meetings (Daily Operations Review, product/process teams)
- Conduct trend analyses, evaluate corrective actions, and monitor effectiveness
- Support continuous improvement initiatives aligned with GMP, quality, and performance KPIs
- Contribute to team projects or initiatives as assigned by the Team Leader or Manager
Your Profile:
- Degree in Bioengineering, Pharmacy, Biology, Biochemistry, Biotechnology, Chemistry, Engineering, or equivalent experience
- Experience as a Qualified Person is a plus
- Previous exposure to manufacturing, packaging, or laboratory environments
- Experience with quality investigations and release of biological products or vaccines is preferred
- Fluent in Dutch and English (written and spoken)
- Strong analytical, problem-solving, and documentation skills
- Excellent communication and stakeholder interaction abilities
- Able to manage time effectively and prioritize tasks in a dynamic environment
Our offer:
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]
