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...

**Summary**: - To be used only for Intern or Student positions. Please enter specific details in the Additional Specifications Details field **About the Role**: **Major accountabilities**: - Work in collaboration with the PS&PV stakeholders to produce compliance reports and complete quality checks to monitor regulatory compliance as well as compliance to...

**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 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...

Bristol Myers Squibb is committed to fostering a diverse and inclusive work environment, where talented professionals can thrive and contribute their expertise.Salary: $120,000 - $180,000 per year, depending on qualifications and experience.About the RoleThis Senior Pharmacovigilance Compliance Manager position plays a critical role in ensuring compliance...

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,...

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,...

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...

Job SummaryWe are seeking a highly skilled Pharmaceutical Safety Associate to join our team at Lifelancer. The successful candidate will be responsible for approving and scheduling reports in the Argus database, ensuring timely submission to health authorities, business partners, and affiliates as applicable.This role requires strong knowledge of...

Job SummaryOracle Life Sciences is seeking a highly skilled Principal Consultant with expertise in Argus Drug Safety Data Migration to join our team. As a key member of our Life Sciences Technical Consulting (LSTC) group, you will be responsible for delivering high-quality services to our customers worldwide.The ideal candidate will have a strong background...

**Major accountabilities**: - Plan and maintain timetables for PSMF production. Maintain list of core and annex contributors, and PSMF signatories plus their deputies. Coordinate production of core PSMF documents in collaboration with internal and external contributors. - Work closely with Manager, QPPV Office to ensure accurate representation of the Sandoz...

Job SummaryThe primary responsibility of this role is to manage patient oriented programs (POP) ensuring compliance with applicable processes and quality standards. The ideal candidate will have experience in clinical pharmacovigilance, medical affairs, or regulatory affairs and be able to communicate effectively across different audiences.Key...

**Summary**: Provide support for medical safety management within the Patient Safety & Pharmacovigilance department, including medical review and assessments of Individual Case Safety Reports (ICSR), aggregate reports, co - authoring safety documents, assisting in providing safety input to regulatory and clinical documents, as well as ad-hoc Health Authority...

**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...

Description WWPS is responsible for ensuring the safety of our medicines: pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy, execution of certain post-marketing commitments and ensuring...

**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...