Beschreibung
We have a contract opportunity to join a major medical device company in Solothurn to ensure the Compliance of their Standard Operating Procedures (SOPs) in accordance to European (CE) and American (FDA) Medical Device regulations, please note that fluent German is essential for the role. The contract is on a full time, onsite 3 month Contract basis and pays an Hourly rate of 75-80 Chf.
A minimum of 2 years of Quality Assurance/Compliance experience for the medical device industry is required for the role, you must have a good understanding of medical device regulations. It is also important to have had prior experience in Technical Writing for the life science industry with experience in using GDP (Good Documentation Practice), this experience may have been with pharmaceutical or biotech company and can be with alternative departments for example supply chain, clinical research or medical affairs.
If you are a German speaking medical device Quality professional who is available on short notice but do not hold all of the above requirements then please feel free to apply for the role. There is a detailed job description available on request.
We understand that you may wish to know more about the responsibilities of the role before submitting an application, please feel free to submit your CV or contact details via this website or email me and I will be happy to answer any questions you may have.
We look forward to hearing from you,
Kind regards,
Michael Kellitt
Michael Bailey Associates AG
Job Code: 109
Key words: Quality Assurance, Quality Management, Qualitat Ingenieur, Quality Engineer, FDA, CFR 510k, Class III, Mechanical Engineer, GDP, Compliance Engineer, Validation, SOPs
Michael Bailey International is acting as an Employment Business in relation to this vacancy.