Medical Device Project Manager 17235
Veritaz AB
📍 Sverige
⏰ Heltid
📋 Vanlig anställning
🗓 Ansök senast 13 maj 2026
✦ Få fler intervjuer
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Skapa ansökan – från 49 kr Gratis att söka · Ingen registrering · 49 kr/mån för obegränsatOm jobbet
Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.
Assignment Description
We are looking for a Senior Project / Program Manager
What You Will Work On
Establish and lead a regulatory gap-closure program across multiple product areas
Translate regulatory gap analyses into structured and actionable work packages
Coordinate cross-functional execution across QA/RA, Engineering, Product, and Documentation teams
Ensure remediation activities follow Design Control requirements (ISO 13485)
Link remediation work to Change Control, CAPA processes, and DHF/DMR updates
Manage dependencies, risks, and resource constraints across multiple workstreams
Provide executive-level reporting on progress, risks, and decision points
Prepare decision materials for steering committees and leadership forums
Drive structured execution and ensure audit readiness across all activities
What You Bring / Required Qualifications
Proven experience delivering regulatory remediation, audit response, or gap-closure programs
Strong knowledge of ISO 13485 and EU MDR
Experience with FDA QSR / QMSR (preferred)
Experience working with design control processes, including retrospective remediation
Ability to coordinate across multiple products and organizational units
Experience working in cross-functional environments with QA/RA, engineering, and product teams
Strong ability to manage complex programs with multiple dependencies
Fluent in English, both written and spoken
Assignment Description
We are looking for a Senior Project / Program Manager
What You Will Work On
Establish and lead a regulatory gap-closure program across multiple product areas
Translate regulatory gap analyses into structured and actionable work packages
Coordinate cross-functional execution across QA/RA, Engineering, Product, and Documentation teams
Ensure remediation activities follow Design Control requirements (ISO 13485)
Link remediation work to Change Control, CAPA processes, and DHF/DMR updates
Manage dependencies, risks, and resource constraints across multiple workstreams
Provide executive-level reporting on progress, risks, and decision points
Prepare decision materials for steering committees and leadership forums
Drive structured execution and ensure audit readiness across all activities
What You Bring / Required Qualifications
Proven experience delivering regulatory remediation, audit response, or gap-closure programs
Strong knowledge of ISO 13485 and EU MDR
Experience with FDA QSR / QMSR (preferred)
Experience working with design control processes, including retrospective remediation
Ability to coordinate across multiple products and organizational units
Experience working in cross-functional environments with QA/RA, engineering, and product teams
Strong ability to manage complex programs with multiple dependencies
Fluent in English, both written and spoken