Medical Reviewer – VAF 432

ProductLife Group is looking for an experienced, French speaking Medical Reviewer.

At ProductLife Group (PLG), we’re a trusted global partner in life sciences, dedicated to improving public health through regulatory excellence and innovation. As a Medical Reviewer, you’ll be part of a growing international team with the opportunity to:

🌍 Collaborate Globally: Work with international teams on diverse regulatory and clinical projects.

🧠 Grow Your Expertise: Deepen your knowledge in pharmacovigilance, clinical trials, and therapeutic areas with professional development opportunities. This role can be a stepping stone to significant career progression in PLG’s rapidly growing pharmacovigilance business unit .

🚀 Develop Within a Dynamic Platform: Be part of a fast-evolving organization that values continuous learning.

🤝 Thrive in a Balanced & Supportive Culture: Enjoy flexible work arrangements and a collaborative environment that supports your well-being.

🏆 Work for a Recognized Leader: Certified as a Great Place to Work, PLG fosters trust, growth, and inclusion.

🌐 Make a Real Impact: Play a key role in advancing public health through meaningful medical review contributions.

Post-Marketing (Pharmacovigilance)

• Support in seriousness assessment including Initial Triage
• Support in causality, medical assessment, MedDRA coding.
• Mentor junior medical reviewers and perform additional review of cases to ensure competency.
• Participate in audits and inspections as required
• Ensure understanding of client needs, conventions and ensure expectations are met and exceeded
• Training and mentoring other team members

• Education: MBBS or MD (Doctor of Medicine) – Specializing in Dermatology

• Experience:
• Experience of SUE assessments
• Cosmetics Regulation Act
• Client communications
• Safety Database experience
• Minimum 5 years experience working for service providers or pharmaceutical company in Pharmacovigilance department

Languages: French AND English (Native/Fully professional); any additional languages are a plus

• Proficiency in Microsoft Office
• Strong understanding of GVP, FDA regulations, and cosmetic regulations and regulatory requirements related to drug/cosmetic safety.
• Deep knowledge of pharmacovigilance principles, adverse event reporting, causality assessment
• Solid medical knowledge and Pharmacology understanding
• MSSO- MedDRA

• Effective written and verbal communication
• Clinical experience (preferred)
• Emotional intelligence, adaptability, and analytical thinking
• Strong organizational skills, reliability, and punctuality
• Experience with safety databases