Compliance Officer

Responsibilities: · Update/correct products related documentation for all departments including production · Coordinate IVDR activities for document completeness as per IVDR requirements · Plan and undertake internal quality audits · Support QA team on documentation update · Coordinate PMS (Post Market Surveillance) activities with internal and external customers · Compilation of product related data for Performance Evaluation Reports (PER) for IVDR compliance · Implement processes as per periodical update of IVDR with appropriate documentation Skills & Qualifications: Masters in Science in Chemistry, Biochemistry, Microbiology or a similar field Good communication skills - oral and written in English, Finnish proficiency will be an added advantage Strong interpersonal skills with the ability to influence others Familiarity with the new European IVDR Directive Knowledge of MS Office tools, and technology related software Knowledge of Medical Devices/IVDR regulatory affairs discipline throughout the product lifecycle, including Design, Development, Labelling, Marketing, Launch and Commercialization Familiarity with Regulatory Authority policies and guidance and apply them as appropriate in product development and commercialization Business orientation and ability to see the business drivers form IVDR perspective Yhteystiedot: Sanchit Ganjoo, [email protected] Hakuohjeet: Please send your resume by email at [email protected] Palkkaus: Salary will depend on experience Ilmoitus jätetty: 14.10.2026 Hakuaika päättyy: 23.10.2026 Työmarkkinatorin ilmoitusnumero: a00c35f6-de6c-4952-8ce4-d24bd53c263b Lähde: Työmarkkinatorin asiakastietojärjestelmä .