Duration: 1 year (extension is possible)
Start date: 1-11-2022
Our client is the leader in the field of biotechnology, deeply value-based in science and innovation to transform new ideas and discoveries into medicines for patients with serious illnesses.
As a Sr. Associate QA/Validation Engineer you will be responsible for the validation of equipment, automation and information systems for the Quality Risk Management.
- Review and approve validation documentation
-Perform process, equipment and IS validation
-Manage ABR’s device responsibilities and ensure alignment with GMP regulations
-Perform final review of technical change control.
-MBO or Bachelor’s degree in Life Sciences or process technology related field
-3 years of experience of working in a pharmaceutical or medical devices environment
-Knowledge of GMP, IS validation and computer compliance
-Preferred experience with CAPAs and Change Control
Are you ready to the next step in your career? Do not hesitate to apply below.