Pharmacovigilance (Pv) (Ra) & Qc

ROLE: Quality Assurance. Pharmacovigilance (PV). Regulatory Affairs (RA) & Quality Control Location: France, Germany, Switzerland, Ireland, and the Czech Republic Pay rate -15-20 Euros/ hour Initially 20 hours per week/ After 1 year 40 hours per week Must have fluent English communication skills. Must be able to face challenging situations Quality...

ROLE: Pharmacovigilance (PV)and Regulatory Affairs (RA) **Location: France, Germany, Switzerland, Ireland, and the Czech Republic** Pay rate -15-20 Euros/ hour Initially 20 hours per week/ After 1 year 40 hours per week Must have fluent English communication skills. Must be able to face challenging situations Pharmacovigilance (PV), Regulatory Affairs...

**Company Description** Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because **Good Health Can’t Wait**. We started in 1984 with a modest...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Job SummaryWe are seeking a highly skilled PV Compliance Specialist to join our team at Bristol Myers Squibb. As a PV Compliance Specialist, you will be responsible for ensuring the safety of our medicines by monitoring safety outputs and ensuring compliance with global regulatory requirements.Key ResponsibilitiesProvide compliance oversight through ongoing...

Job SummaryWe are seeking a highly skilled Pharmacovigilance Quality Risk Manager to join our team at Bristol Myers Squibb. As a key member of our Worldwide Patient Safety group, you will be responsible for ensuring the safety of our medicines through ongoing monitoring of safety outputs and compliance with global regulatory requirements.Key...

Key ResponsibilitiesAs a Senior Pharmacovigilance Compliance Specialist at Bristol Myers Squibb, you will be responsible for ensuring the safety of our medicines by ensuring compliance with global regulatory requirements. You will have a strong scientific background in a life science related field and 5 years of pharmaceutical industry experience, including...

Job SummaryWe are seeking a highly skilled PV Compliance Specialist to join our team at Bristol Myers Squibb. This individual will be responsible for ensuring compliance with global regulatory requirements and ensuring the quality and safety of our medicines.Key ResponsibilitiesProvide compliance oversight through ongoing monitoring of safety outputs created...

Job Title: PV Compliance and Quality Risk Management SpecialistThe Worldwide Patient Safety (WWPS) group is responsible for ensuring the safety of our medicines through pharmacovigilance and pharmaco-epidemiology deliverables. This includes single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management...

Job OverviewBristol Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. We are seeking an experienced Senior Pharmacovigilance Specialist to join our team.About the RoleWe offer a competitive salary of $120,000 per annum, plus benefits. As a Senior Pharmacovigilance Specialist, you will be responsible...

Job SummaryThe Senior Pharmacovigilance Compliance Specialist will be responsible for ensuring the safety of our medicines by ensuring compliance with global regulatory requirements. This includes monitoring safety outputs to ensure quality excellence and compliance with worldwide GVP regulations, guidance, and inspectorate expectations.Key...

Job SummaryWe are seeking a highly skilled Senior Pharmacovigilance Compliance Specialist to join our team at Bristol Myers Squibb. As a key member of our Worldwide Patient Safety group, you will be responsible for ensuring the safety of our medicines and ensuring compliance with global regulatory requirements.Key ResponsibilitiesProvide quality oversight...

Job SummaryAs a key member of the Worldwide Patient Safety (WWPS) group, the Senior Pharmacovigilance Compliance and Quality Manager will play a critical role in ensuring the safety of our medicines. The successful candidate will be responsible for quality, compliance, and inspection readiness activities in WWPS through ongoing monitoring of safety outputs,...

Description The Worldwide Patient Safety (WWPS) group is responsible for ensuring the safety of our medicines: WWPS group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy,...

Job SummaryWe are seeking a highly skilled and experienced professional to join our team as a PV Compliance and Quality Specialist. In this role, you will be responsible for ensuring the quality and compliance of our pharmacovigilance activities, including safety database case processing, quality monitoring, and compliance with global regulatory...

390691BR **RA Coordinator**: India **About the role** Your responsibilities include, but are not limited to: - Independently manage and prepare routine Health Authority submissions including Annual Reports, DSUR, New Protocol Submissions, Protocol Amendment, and New Investigator Submissions to ensure timely submissions in accordance with the FDA...

Description The Worldwide Patient Safety (WWPS) group is responsible for ensuring the safety of our medicines: WWPS group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy,...

Job SummaryWe are seeking a highly skilled Pharmacovigilance Quality Assurance Specialist to join our team at Bristol Myers Squibb. In this role, you will be responsible for ensuring the quality and compliance of our pharmacovigilance activities, including safety database case processing and quality monitoring.Key ResponsibilitiesPerform ongoing monitoring...

Analysis of the campaigns, investigations, and related analyses with trouble shooting - Execution of the Analytical method validation as per the protocol - Preparations of equivalency reports, transfer protocols & reports, investigation protocols & reports etc. - Maintenance of lab compliance such as calibration schedules etc, preparation of SOPs and other...