Quality system expert Specialist Medical Devices

Major Acountabilities are:

• Ascertaining of GMP and regulatory compliant processes within the manufacturing group and its suppliers
• Implementation of current authority regulations processess in the aras of Medical Devices
• Preparation and follow-up of inspections from health authorities, customers and internal activities
• Coordination & communication with external functions eg othr manufacturing sites, supply chain management, regulatory cmc.
• Local and global project participation or lead
• Support in qualification of suppliers/manufacturers
• Perform external audits and establishing/maintenance Quality agreements with Medical device suppliers and component suppliers

Your Profile:

• university degree in Mechanical Engineering, Material Technology, or chemistry or Pharmacy, or equivalent
• several years experience in the medical device industry or direct experience in working with medical devices within the pharma environment in relevant quality control or quality assurance or regulatory functions.
• Fluent English and basic German (fluent German would be a plus)

If this interesting position appeals to you, please do not hesitate to apply today! either through our online portal or via email.

r 20004642