Regulatory Compliance Jobs in Niš

Key Responsibilities:Prepare and manage marketing authorization (MA) submissions including the preparation of local administrative documents quality control (QC) and compilation. Provide ad hoc regulatory advice on submission packages in the postauthorization stage of the medicinal pr More...

The Assistant Regulatory and PV Network will support the team with administrative tasks including tracking data retrieval planning document organisation and archiving to ensure smooth daily operation of the PrimeVigilance RA and PV Network department.Candidates will have the oppo More...

Provides leadership and management of the QA team and business partners responsible for overseeing Quality Management System activities Provides input into the internal global audit program identifying risks and determining the number and types of audits to be conducted eac More...

The Assistant Regulatory and PV Network will support the team with administrative tasks including tracking data retrieval planning document organisation and archiving to ensure smooth daily operation of the PrimeVigilance RA and PV Network department.Candidates will have the oppo More...

POSITION SUMMARYThe Associate Quality Projects and Metrics supports the Quality Projects and Metrics Team inensuring that PrimeVigilances Quality and Compliance Metrics are compiled analyzed and reported incompliance with global regulations legislation and PrimeVigilance requirements. More...

Contract Type: Interim (6 months with potential for a 6month extension)Work Model: Remote (with two business trips lasting three days each)Are you passionate about electric powertrains and innovative automotive solutions We are seeking a highly skilled Architecture System Engineer to More...

Assures and exerts activities leading to effective cooperation with clients in the area of literature monitoringContributes to achieving companys goals and objectivesEnsures that the Literature Screening responsibilities and activities are managed in a costefficient manner of the high 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...

This is an opportunity for new graduates to start and develop their career within drug safety. The Medical Writing Assistant will be working as part of a medical writing team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilanceHandling (trackin More...

The 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 safety. Th More...

57 years of experience  Fulltime  English UpperIntermediate (B2Requirements Experience of work in enterprise environment and good understanding of enterpriselevel system design (Hardened environment Centralized systems Security Operation and Maintenance ITILaware More...

This is an opportunity for new graduates to start and develop their career within drug safety. The Medical Writing Assistant will be working as part of a medical writing team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilanceHandling (trackin More...

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...

The 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 safety. Th More...