Project Qualification Engineer (m/f/d)

As a member of the Quality Team, you are responsible for testing our products and technologies against the requirements of the pharmaceutical industry in coordination with technical development and product and project management. You advise our customers with your expertise on their questions regarding GMP compliance of the products and ensure that our equipment and manufacturing processes are continuously qualified and validated.

Your tasks

• You ensure compliance with applicable quality standards in customer projects and internal development projects
• You are responsible for carrying out risk analyses and creating test protocols/reports
• You will supervise various qualification and validation tasks and coordinate product analytics
• You support project management in customer project execution
• Support with general quality management tasks, such as document management, deviation investigations and auditing, rounds off your area of responsibility

Education

• Technical or scientific background
• Relevant professional experience, preferably in the pharmaceutical industry, medical technology, mechanical engineering / (bio-) process engineering or comparable
• Experience in quality management or knowledge of the ISO 9001 standard and/or GMP desirable
• Ideally relevant experience in pharmaceutical qualification projects
• Business fluent in German and English
• Proactive, structured, solution-orientated way of working
• Very flexible, independent, results-orientated
• Ability to prioritize and work under time pressure
• Strong customer orientation and communication skills