Medical Device Expert - Human Factor

Medical Device Expert - Human Factor wanted for our Basel based client in the pharmaceutical sector. Your experience/skills: Degree in a proper subject along with relevant working experience in the pharmaceutical or medical device industry Experience in planning and writing technical documentation with Medical Device Design Control for Medical Devices and product combinations Excellent Project Management skills Experince in ISO 13485, ISO14971, MDD and QMS for Medical Devices Ideally know how of Auto Injectors and Safety Devices Languages: fluent German and English both written and spoken Your tasks: Writing, reviewing and approving deliverables (e.g. procedures) and related tools (e.g. IT) to ensure GMP compliance Managing quality problems and technical matters as well as ensuring global standards and policies Releasing of Medical Devices for clinical studies and commercial use Supporting Medical Device Risk Management to minimize impact on global supplies and patients as well as representing MD Quality in initiatives and cross divisional projects Meeting internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority requirements, SOPs, HSE, etc.) Contributing to internal compliance policy and commenting to regulations Start: ASAP Duration: 15MM+ Location: Basel, Switzerland Ref.Nr.: BH11622 Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number. Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work permit holders for Switzerland. Going the extra mile… New to Switzerland? In case of successful placement, we support you with: All administrative questions Finding an apartment Health - and social insurance Work permit and much more