Sr. QMS Specialist
Currently working with a Biotech Client in Switzerland who are in need of support from a Sr. QMS Specialist for ongoing high-level projects. This is an opportunity to work with a fast-paced organisation with cutting edge-technology for a 6-month contract (extension expected for additional 6 months). Interview + offer will take place this week and next, so get in touch ASAP if interested.
Responsibilities:
- Support the quality improvement activities across site by supporting project groups to execute necessary projects.
- CAPA follow up, change management, documentation management
- Collect data from different stakeholders for quality management review
- Support the development of a quality improvement culture.
- Support the development and execution of strategies to strengthen the Quality culture within other site functions.
- Challenge constraints on operational activities to remove discrepancies and non-value adding process steps.
- Review Approve and Close QMS systems records
Requirements:
- 7+ years of experience within a GMP environment
- Expertise with risk management is an asset
- Good knowledge SAP, MES, DMS, and Trackwise
- Autonomous worker and team player
- Fluent in English, German is an asset
Position: Sr. QMS Specialist
On-site: 4 days/week
Location: Valais, Switzerland
Start Date: Immediately or by agreement