Together, we are creating a dynamic products and services company, dedicated to supporting research that makes a real difference to people's lives.

Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today. Chances are, you or someone you know has benefitted from a medicine or medical device that Covance helped develop.

We are committed to providing our customers with exactly what they need, from outsourced single studies and the supply of animal models and services, to managing complex programs and the development of long term strategic partnerships.

The QA team, based in Munich, has an immediate need for a Senior QA Auditor to join the growing team.

Based in Covance offices or remotely (home-based), the Sr. Auditor I role is responsible for leading internal and external QA audits per SOPs and Master Audit Plan, assuring that audited systems, processes and their outcomes comply with applicable international and national regulations and guidelines, and fulfill client and Covance requirements.

The position assures that audits assigned are completed on time and with budget, including audit reporting and CAPA follow up and closure.
Education/Qualifications:

• University/College Degree (BA/BS) preferred
• Understanding of the drug development process
• Knowledge, understanding and experience applying ICH guidelines, GCP's including applicable regulatory requirements for the conduct of clinical development programs

Experience:

• Excellent written, oral and presentation skills
• Proven experience of working in a global organisation
• Ability to handle multiple priorities