Pharmacovigilance (Pv) (Ra) & Qc

3 days ago

Hyderabad Telangana, India Madagoni LLC Full time

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 Assurance (QA), Pharmacovigilance (PV), Regulatory Affairs (RA), and Quality Control (QC) within the pharmaceutical and biotechnology sectors in France, Germany, Switzerland, Ireland, and the Czech Republic:
Quality Assurance (QA)
- Role: Ensure that pharmaceutical products and processes meet regulatory standards and company policies.
- Typical Responsibilities: Developing and implementing QA policies, conducting audits, reviewing documentation, ensuring compliance with GMP (Good Manufacturing Practices).

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.

Quality Control (QC)

Role: Perform tests and inspections to ensure that products meet quality standards and specifications.

Typical Responsibilities: Conducting laboratory tests, monitoring production processes, documenting results, and ensuring compliance with quality standards.

Schedule:

- Day shift

**Experience**:

- total work: 1 year (preferred)

Work Location: In person

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