Materials Controller

For our customer in Solothurn we are looking for a project for a:

Materials Controller

Duties and responsibilities:

- With oversight from the Core Team Leads, determine and report on the state of compliance of the quality system versus regulatory standards for Medical Device Industry (ISO, FDA, etc.)
- Audit sites' procedures to the standards and report out on finding (both current state and retrospectively)
- Make recommendations to achieve compliance where shortfalls are found
- Provide Audit report as directed
- Perform verifications of effectiveness as necessary
- Be willing and able to travel to other sites in Europe as required
- Thorough understanding of GMP and GCP guidelines

Experience:
- Minimum 4 years quality/compliance experience in the medical device or pharmaceutical industries
- Prior experience in medical device/pharmaceutical remediation preferred
- Familiarity and interaction experience with regulatory auditing bodies preferred
- Documented training in FDA QSR, ISO 13485/9001 required
- Proficient in the use of Microsoft Office, MS Visio and/or MS Project are a plus
- Some ERP knowledge (preferable Agile, JD Edwards and SAP)

Are you interested in this position? Then we looking forward to receive your application.