Your new role
As QC officer you will have a range of different responsibilities, which will include:
What you'll need to succeed
- Planning activities associated with quality operations
- Admin work in line with routine QC support work and investigations
- Compliance with pharmaceutical laws and regulations
- QA guidelines are followed in QC activities
- Deviations/OOS-OOT/ temporary changes/ PTP
- Report planning in line with stability studies
HBO in Life Sciences with 2-3 years’ experience in a cGMP environment such as QA/QC. R&D and medical devices. Knowledge of pharmaceutical laws and regulations. If you have previous experience in quality related documentation it is considered a plus. Ability to follow changes in laws and regulations and assess them for applicability to the organisation. Conversational Dutch and excellent English are required.
Your new company
Prothya Biosciences, an organisation committed to providing high quality plasma derived products. This is done through complex methods used to isolate proteins from blood plasma to transform them into life-saving medicines. Not only are they committed to patient care, they also develop advanced solutions for client partners. Prothya colleagues go the extra mile to deliver top quality patient care worldwide!
What you'll get in return
Hays Detachering | This is a project that will start with a contract for 6 months through Hays. Extension to stay within the department is anticipated. At this position, you will get a competitive salary and your travel expenses are covered.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1045849