QA COMPLIANCE REVIEWER
TMC
- Bruxelles
- CDI
- Temps-plein
- You act as the point of contact within the team and provide assistance to other departments on matters of compliance.
- You are punctual in following up on possible issues and change-related documentation.
- You rectify daily deficiencies within reviewed documentation, strictly following cGMPs and SOPs.
- You ensure MES project compliance with procedures and regulations and instigate non-conformance investigations.
- You convey up-to-date status reviews to the team, consistently updating tracking spreadsheets and reports.
- You coordinate with project teams to refine and expedite the batch records cycle time.
- You compile production information for OOS, Deviation, and CAPA logs.
- You ensure the availability of production documents and perform quality review for executed batch records.
- You have a Master's degree in Biomedical Sciences, Bioscience engineering, Biochemistry, Industrial Pharmacy, …
- A first experience in a pharmaceutical or biotech environment is a plus.
- You have an eye for detail.
- You have strong analytical and problem-solving skills.
- You are able to work independently and as part of a team.
- Accuracy in e.g. administration is one of your strong points.
- Fluent in Dutch and English.
- You will have a permanent employment contract, offering you stability and security
- You will get to know your market value and have a share in the profit your work generates thanks to the individual profit sharing
- We will support you with one-on-one coaching and training designed to help you develop your entrepreneurial skills
- The competence cells structure provides you with a strong meaningful and relevant network
- The entrepreneurial lab: a playground for new ideas and a potential launching for start-ups