Corporis Medical is hiring a Quality Assurance Specialist/ Project Manager
Do you have a Quality mindset by nature? Do you already have some experience in the medical devices industry and are you looking to join a start-up company? Then this might be the opportunity you are looking for:
Being Corporis Medical’s QA Specialist your main role is to maintain its Quality Management System according to ISO 13485 standards. You assure compliance with all applicable regulations and procedures and support new product design / development and testing with design control, risk assessments and -reviews by providing QA technical expertise. Also reviewing and approving documentation for design history files, technical files and other regulatory submissions and conducting internal audits and external supplier audits and batch records are part of the job. You will maintain and track corrective and preventive actions and provide direct and regular communication to senior management on progress, opportunities & issues.
BSc / MSc in Biomedical Sciences / Engineering / Medicine or another relevant field.
1-3 years of experience in the field of Medical Devices Industry.
Good understanding of QA and QM systems and the ability to guide the rest of the organisation in this matter.
Understanding of product- and process development in medical devices.
Strong and proven project management skills and highly structured way of working.
Understanding of and experience with regulatory approval of medical devices (EU/USA).
Excellent communication skills, both in English and Dutch.
If you want to know more about Corporis Medical, the challenges in the job or want to apply at once, get in touch or send your resume and motivation letter to firstname.lastname@example.org before December 21st 2019.
Health Campus Maastricht, The Netherlands.