Our client is active in the biopharmaceutical markets and they are looking to strengthen their Quality team in Switzerland.
- You will support QA activities connected to the facility engineering and validation
- You will provide QA oversight of the change control system
- You will continuously improve, streamline, review & approve change controls directly with functional areas
- You will provide quality oversight of validation activities
- You will work directly to review and approve GMP documentation and facilitate ongoing lifecycle management
- You will develop and manage all validation policies, procedures, and protocols
- You will provide general QA support for various departments
- You should have a Bachelor degree as a minimum
- You should have experience in a QA cGMP environment ideally within Biopharmaceuticals or equivalent
- Knowledge of regulatory and GMP standards for local authorities
- Experience with computer system validation and/or qualification of enterprise systems is an advantage
Interested? Please do not hesitate in sending your CV and/or the best contact details for yourself to firstname.lastname@example.org and our team of skilled consultants would be very happy to contact you with more details.
Proud to be working in partnership with Talentory AG
To apply for this job email your details to email@example.com.