
Pharmacovigilance (Pv) (Ra) & Qc
1 week ago
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 (RA) within the pharmaceutical and biotechnology sectors in France, Germany, Switzerland, Ireland, and the Czech Republic:
Pharmacovigilance (PV)
- Role: Monitor, assess, and report on the safety of pharmaceutical products to ensure they are used safely and effectively.
- Typical Responsibilities: Collecting and analyzing adverse event data, preparing regulatory reports, ensuring compliance with safety regulations.
Regulatory Affairs (RA)
- Role: Ensure that products meet all regulations and standards required for approval and marketing in various regions.
- Typical Responsibilities: Preparing and submitting regulatory documents, interacting with regulatory agencies, ensuring compliance with local and international regulations.
**Note**
Pay: Up to ₹100,000.00 per month
Schedule:
- Day shift
Work Location: In person
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