{"id":30959,"date":"2026-04-17T00:00:00","date_gmt":"2026-04-16T22:00:00","guid":{"rendered":"https:\/\/www.keyman.se\/sv\/uncategorized\/developer-for-ai-supported-medical-device-mdr-to-karolinska-inatitutet-15416\/"},"modified":"2026-04-17T00:00:00","modified_gmt":"2026-04-16T22:00:00","slug":"developer-for-ai-supported-medical-device-mdr-to-karolinska-inatitutet-15416","status":"publish","type":"post","link":"https:\/\/www.keyman.se\/sv\/data-it\/developer-for-ai-supported-medical-device-mdr-to-karolinska-inatitutet-15416\/","title":{"rendered":"Developer for AI supported medical device (MDR) to Karolinska Inatitutet"},"content":{"rendered":"\n\n\n\n\n\n\n\n\n\n\n\n
Roll<\/strong><\/td>\nFullstackutvecklare<\/td>\n<\/tr>\n
Kompetensomr\u00e5de<\/strong><\/td>\nData\/IT<\/td>\n<\/tr>\n
Startdatum<\/strong><\/td>\n2026-04-27<\/td>\n<\/tr>\n
Slutdatum<\/strong><\/td>\n2026-11-01<\/td>\n<\/tr>\n
Omfattning<\/strong><\/td>\n100%<\/td>\n<\/tr>\n
Ort<\/strong><\/td>\nStockholm or EU<\/td>\n<\/tr>\n
Land<\/strong><\/td>\nSweden<\/td>\n<\/tr>\n
Sista svarsdatum<\/strong><\/td>\n2026-04-22\u00a0(Offerter kommer att behandlas l\u00f6pande)<\/em><\/td>\n<\/tr>\n
Kontaktperson<\/strong><\/td>\nMaja Denham-Smith (maja.denham-smith@keyman.se<\/a> | 070-555 72 21)<\/td>\n<\/tr>\n
Referensnummer<\/strong><\/td>\n#15416<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
\u00d6vergripande uppdragsbeskrivning<\/h5>\n

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We are looking for an IT consultant for the further development of medical device software class IIa, with a focus on MDR compliance, technical documentation, usability, cybersecurity and AI governance, and has a basic understanding of the basics of clinical psychology. The project will support an MDR software and the requirements include software verification\/validation, data protection, risk management and regulatory-sustainable documentation. The supplier must be able to demonstrate documented experience in software development, regulatory technical documentation, cybersecurity, AI-related data governance and usability work in a regulated environment.<\/p>\n

The supplier shall specify a fixed total price for the entire assignment in the quotation; however, invoicing will be made in installments over the course of the period.<\/p>\n

The start date is flexible. There is a preference to commence the assignment as soon as possible.<\/p><\/div>\n<\/p>\n

Skallkrav<\/h5>\n

Experienced IT consultant for development of medical device software class IIa, with a focus on MDR compliance, technical documentation, usability, cybersecurity and AI governance.<\/p>\n

B\u00f6rkrav<\/h5>\n

Basic understanding of clinical psychology<\/p>\n

\u00d6vriga krav<\/h5>\n

Briefly describe in the comment fields for the mandatory and desired requirements how the consultant meets these.
\nPlease attach the CV in Word format under the Documents tab. The CV is an important part of the evaluation of the consultant and must clearly demonstrate that the consultant has the competence and experience required for the specific assignment.
\nThe quotation for this assignment must be submitted via KeySourcingTool. Responses submitted by email will receive limited feedback.
\nThe supplier certifies that consultant and professional liability insurance is in place and covers this type of assignment in accordance with industry standards.<\/p>\n

Personliga egenskaper<\/h5>\n

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\u00d6vrig information<\/h5>\n

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Option to extend part-time, up to and including 2028-02-01.<\/div>\n<\/p>\n

 <\/p>\n

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