As the QA Officer you will be responsible for maintaining and improving the QMS document control system including the documentation for private label product production.
You will proactively support operational staff to comply with the QA requirements. You will be our gatekeeper in risk management, vigilance processes and complaint management.
Update procedures for self-certification for class I medical devices and certification in cooperation with the Notified body. Monitoring external changes to the related standards and assess impact for Medeco B.V. is also a main aspect of the job.
You will be responsible for the timely execution and follow up of internal and external audits, following the Medeco B.V. quality system.