Quality/Validation Engineer in Grenchen
Quality/Validation Engineer - Grenchen, Switzerland
Alex Tosney is recruiting for a Quality/Validation Engineer to join a global medical device company at their site based in Grenchen on a contract basis for 6 months.
The Role: The primary purpose of this position is to support the transfer of production capabilities to an external supplier.
Further responsibilities will include:
- Process validation and verification activities.
- CAPA management.
- GMP and FDA compliant documentation tasks.
- Validation of production processes.
In order to be considered for this role, you will be required to have the following qualifications, skills and experience:
- Degree in Engineering (preferred), or in a related technical/scientific discipline is required.
- Problem solving techniques including 8D, root cause analysis and cause and effect analysis. Experience in CAPA execution and management.
- Experience within a regulated environment (e.g. FDA, ISO 13485 regulated), ideally in Med-tech.
- Experience in Change Control, Manufacturing/Product Transfers, Outsourcing Initiatives.
- Experience with project management.
- Language: English and German mandatory.
This is an excellent opportunity to join a world leader in the medical device field.
For more information or to apply for this position, please contact Alex Tosney on 0041 (0) 782 508 443 or email atosney@ckqls.ch. Please quote reference 45665 in all correspondence.
