Quality and Regulatory Compliance Auditor (x|f|m) - Hybrid

We are looking for a Quality and Regulatory Compliance Auditor to join our Regulatory Affairs and Compliance department. The role involves steering and management of bioprocess solution operations business unit level quality audit program, providing specialist input to the regulatory affairs team, and ensuring regulatory requirements are fulfilled.

Requirements

• Successfully completed Master's degree in a relevant scientific discipline
• First years of experience at supervisory level in a regulated environment
• Competence and qualifications for quality and regulatory elements for medical device and ISO related certifications
• Proven ability to work effectively in cross-functional and international teams
• Experience with notified bodies and auditing processes
• Qualification to act as an auditor in medical device manufacturing industry
• Deep knowledge in interpretation of regulations, guidelines, policy statements, etc.
• Strong interpersonal skills and ability to deal with a variety of personnel
• Advanced organizational skills and ability to prioritize workload
• Business fluent in German and English (oral and written) and willingness to travel (approx. 20%)

Benefits

• Personal and Professional Development
• Work-life balance
• Attractive compensation
• Large, modern campus
• Making an impact right from the start
• Welcoming Culture