Quality Associate (Contract)
HybridRolle, Vaud, Switzerland
Job Summary
Conduct ongoing reviews of open and historical Non-Conformities to ensure audit readiness, manage Corrective and Preventive Actions from root cause analysis through effectiveness verification, and support Change Control Process activities. Partner with cross-functional teams including Supply Chain, Procurement, Data Science, and IT to gather evidence, document conformity, and close out actions on time. Identify emerging non-conformities proactively, assessing risk and recommending appropriate remediation while maintaining accurate records in Veeva and Jira. This hybrid role in Rolle, CH requires at least three days per week in the office and runs as a temporary contract until May 31, 2027. You will join a team dedicated to democratizing data-driven medicine for cancer and rare disease patients globally.
Required Qualifications
- Working knowledge of CAPA, NC, CCP and other quality documentation processes
- Direct experience within a Quality Control / Quality Assurance function
- Experience within a similar scientific, medical or pharmaceutical environment
- Experience with ISO 9001 and ISO 13485 standards
- Systems experience with ticketing and document management tools
- Experience with Veeva & JIRA
- Fluency in English (both written and spoken)
- Ability to include CV in English
Desired Qualifications
- Experience within a similar scientific, medical or pharmaceutical environment
- Experience with Veeva & JIRA
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