Medical Devices Jobs in Poland

We currently have an exciting opportunity at SGS for a Medical Devices Lead Auditor & Training Specialist to join our highly successful Global Medical Device team.In this role you will be reporting directly to the Global Medical Devices Technical Training Manager.Your role wi More...

Are you ready to take your career to the next level If you have a strong background as a Product Assessor within an EU notified body conducting MDD/MDR technical documentation review then we have an exhilarating opportunity for you!Join our dynamic team at SGS and become a Senior Prod More...

We currently have an exciting opportunity at SGS for a Product Assessor Orthopaedic and Dental to join our highly successful certification division.Working as a member of our Medical Device team reporting directly to Global Medical Devices Technical team manager you will manage a tea More...

Are you ready to take your career to the next level If you have a strong background as a Product Assessor within an EU notified body conducting MDS technical documentation review then we have an exhilarating opportunity for you!Join our dynamic team at SGS and become a Software & More...

Our Customer is looking for a Technical Specialist with expertise on mobile devices who needs to work in Hybrid mode only in Krakow Poland. Applicants from other parts of Poland must agree to travel to 23 days to Krakow for this role.Background check: required preonboardingTechnical R More...

Our Customer is looking for a Technical Specialist with expertise on mobile devices who needs to work in Hybrid mode only in Krakow Poland. Applicants from other parts of Poland must agree to travel to 23 days to Krakow for this role.Background check: required preonboardingTechnical R More...

Job DescriptionThe Medical Reviewer II is responsible for medical review of lCSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client.For the Client:To review a More...

As a Product Assessor you will be responsible for conducting comprehensive assessments of Cardiovascular and Soft Tissue products ensuring technical file reviews adhere to all applicable requirements including the European Medical Device Regulation (MDR) Medical Device Directive (MDD) More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in WarsawResponsibilities:Medical point of contact for internal project team study sites and st More...

The Medical Reviewer I is responsible for medical review of lCSRs and literature review writing of signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client. Responsibilities include:To revie More...

Therapeutic area: OncologyTerritorial scope (districts): lskie maopolskie witokrzyskie podkarpackie lubelskie.The Medical Science Liaison (MSL) is a nonpromotional field based scientific expert in a given therapeutic area(s) that strategically supports the medical and scientific objec More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in WarsawResponsibilities:Medical point of contact for internal project team study sites and st More...

Responsibilities include:To review and approve postmarketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Com More...

For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e More...

The Quality Management Officer is responsible for ensuring that Quality Events (QEs) and Corrective and Preventative Actions (CAPAs) are completed in accurate and timely fashion and are managed in compliance with global regulations legislation and PrimeVigilance requirements.Lead the More...

Market compliance expertise: Stay informed on regulations (MDR/IVDR FDA GMP) relevant to the healthcare industry Identify solutions to help clients achieve faster market entry and regulatory compliance Proposal development: Analyze potential clients needs Deve More...

Clinical Study Project Manager Drive Innovation in Medical ResearchAre you passionate about advancing medical research and bringing innovative healthcare solutions to the world Do you thrive in a dynamic fastpaced environment where collaboration and strategic execution are key If so More...

International and country level medical engagement projects management (internal and external scientific events HCPs logistics management scientific communication projects).Support and lead defined stages in the defined geographies Medical Programs management: Managed Access (compassi More...

PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in Polish and English.  Responsibilities  To provide approved responses to med More...

Location: Germany (Various Locations)We are seeking medical doctors specializing in internal medicine (m/f/d) with proficiency in German (at least B2/C1 level) to join leading German hospitals and occupational health centers. This opportunity is open to candidates within the EU and ou More...