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Post Market Surveillance Manager / Clinical Affairs Manager

Inion Oy is a medical devices company focused on the development and commercialization of innovative biodegradable and bioactive surgical implants.  Inion's products for Speciality Orthopaedics, Sports applications, Craniomaxillofacial and Spinal applications are used daily in over 40 countries around the world. Inion has state of the art product development and manufacturing facilities in Tampere and a subsidiary in the USA. We are now strengthening our organization with the position of

Post Market Surveillance Manager / Clinical Affairs Manager

You will be responsible for the post market surveillance activities in accordance with the EU requirements and Inion's PMS plan, and for the post market technical files for Inion products. The work includes planning, resourcing and managing post market clinical follow up studies, and other PMS data collection, updates of risk management files and clinical evaluation reports.  You will join the team for EU MDR transition work for current and future product families. 
Suitable background is minimum 5 years of work experience in the regulatory affairs of medical devices and academic degree of education. Clinical background or CRA experience is an  advantage. Fluent written and spoken English, and ability to create professional medical/technical/ scientific documents and reports is a requirement.

We are looking for a person with internal motivation, initiative for problem solving, good eye in prioritization of tasks as well as good interaction skills for utilizing the potential in teams. The job typically includes several projects in parallel and bringing them into the finish in time. 

For more information, please call or email Kati Marttinen:, +358 40 841 6217. Send your application with CV and salary proposal  to


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