Industrial Safety Jobs in Prague

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/or reviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs. PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Phys More...

Validation engineer is responsible to test that the manufactured Power Management IC is functionally correct in the lab environment. The engineer needs to understand the functional specification of the IC devise the appropriate validation techniques for all the features and create val 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...

Validation engineer is responsible to test that the manufactured Power Management IC is functionally correct in the lab environment. The engineer needs to understand the functional specification of the IC devise the appropriate validation techniques for all the features and create val More...

The Senior Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs writing and reviewing signal detection reports writing and/or reviewing aggregate reports (DSURS PSURS/PBRERs/PADERS ACOs responses to regulatory authority requests) writing and/or reviewing risk 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...

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 PragueResponsibilities:Medical point of contact for internal project team study sites and st 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 Senior PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug saf More...

Renesas is deploying a universal ticketing system based on Atlassian products (JIRA / Confluence)  for customer support worldwide: used daily by thousands of customers and Renesas Employees (Field Application Engineers & factory Application Engineers).  As a member of t More...

The Senior PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug saf 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...

Renesas is deploying a universal ticketing system based on Atlassian products (JIRA / Confluence)  for customer support worldwide: used daily by thousands of customers and Renesas Employees (Field Application Engineers & factory Application Engineers).  As a member of t More...

This is an exciting opportuniy for a freelancer / consultant to join our team as a Person Responsible for Local Literature Screening at 0.5 FTE.By working with us you will have the opportunity to work in an international team.Main responsibilitiesPerforming local scientific literature More...

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.Site ManagementExchanges data documents and other project relevant information between investigative sites site vend More...

Providing support to other activities undertaken by the project team on behalf of the client andthe companyPerforming activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to):Processing Individual Case Safety Reports (ICSRs) fro More...

As a Quality Control Inspector youll be reporting to an Operations Manager and working as a part of our Operations team. At QIMA the role of Operations is to deliver our industryleading services to our clients while ensuring that all the work is performed to the QIMA standard of quali More...

Join our team of experts in regulatory submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Hybrid working arrangement in Prague the Czech RepublicYour role:Pr More...

As a Quality Control Inspector youll be reporting to an Operations Manager and working as a part of our Operations team. At QIMA the role of Operations is to deliver our industryleading services to our clients while ensuring that all the work is performed to the QIMA standard of quali More...

HR AdministrationAs an HR Admin you will play a crucial role in supporting our HR functions. Each month youll help prepare salary documents process employee hires manage employee records and communicate with staff on these matters. Youll also handle administrative tasks related to med More...