Pharmacovigilance Auditor – Freelance, 1FTE or 0.6 FTE and above

This is a fully remote position, open to applicants in Serbia, +1 more country.

📋 Description

• Plan, prepare, execute, report, and follow up on various Pharmacovigilance audits.

• Develop and monitor CAPA (Corrective and Preventive Action) plans.

• Conduct audits in compliance with regulatory standards and Good Pharmacovigilance Practice (GVP).

• Undertake GVP quality assurance initiatives for clients in the pharmaceutical and biotechnology sectors.

• Perform both remote and on-site audits, which may involve travel across Europe.

⛳️ Requirements

• Proven experience in leading and conducting internal and external Pharmacovigilance audits for diverse stakeholders.

• In-depth knowledge of national and international Pharmacovigilance laws and guidelines.

• Skilled in project management with a track record of timely deliverables.

• Capable of identifying problems and providing solutions in a practical manner.

• Willingness to travel for audit purposes.

• A Bachelor’s Degree in Life Sciences is preferred.

🏝️ Benefits

• Freelance position available with options for full-time (1 FTE) or part-time (0.6 FTE and above) work.

• Opportunities for professional development encouraged.

• A supportive and collaborative work environment.

• Chance to make a significant impact within the pharmaceutical and biotechnology fields.

• A diverse and inclusive workplace where every individual's voice matters.

• Collaborate with experts in clinical research, pharmacovigilance, and quality consulting.