Local Safety Officer

Make a meaningful impact on global healthcare — and grow your career while doing it. At ProductLife Group, you’ll join an innovative, forward‑thinking team operating across the world to shape the future of life sciences through expertise, collaboration, and purpose‑driven work.

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Job Description :

About ProductLife Group

ProductLife Group (PLG) is a global consulting and outsourcing organization specialized in supporting the life sciences industry throughout the entire product lifecycle. We provide expertise in regulatory affairs, pharmacovigilance, quality, medical information, and compliance services to pharmaceutical, biotechnology, and medical device companies worldwide.

Position Overview

We are seeking a Local Safety Officer to support our pharmacovigilance activities in France on behalf of our clients. The successful candidate will act as a local pharmacovigilance expert and key contact for French regulatory authorities, ensuring compliance with local and international pharmacovigilance requirements.

This role requires strong pharmacovigilance knowledge, experience in local case management activities, and excellent communication skills to effectively collaborate with clients, health authorities, and internal stakeholders.

Key Responsibilities

Local Safety Officer Activities

• Act as Local Safety Officer for PLG clients in France.
• Serve as a local pharmacovigilance contact and liaison with French regulatory authorities.
• Support Local Pharmacovigilance Person (LPPV) responsibilities where applicable.
• Ensure continuity of local vigilance activities and regulatory compliance.
• Maintain awareness of evolving French pharmacovigilance regulations and requirements.
• Notify local authorities of appointments and maintain required documentation.
• Communicate professionally with clients, authorities, and stakeholders within agreed timelines.

Pharmacovigilance Operations

• Perform receipt, processing, translation, quality control, tracking, and follow-up of Individual Case Safety Reports (ICSRs).
• Support local safety case management activities in compliance with applicable regulations and client requirements.
• Perform local regulatory safety submissions when required.
• Conduct reconciliation activities to ensure complete handling of vigilance reports.
• Support local medical information services when applicable.

Literature & Regulatory Intelligence

• Monitor local French literature and journals for safety information related to client products.
• Perform quality control and tracking of literature monitoring activities.
• Assist in the selection and review of local journals.
• Monitor French regulatory authority websites for safety updates and legislative changes.
• Track safety-related announcements and communicate relevant findings to clients.

Quality & Compliance

• Create and maintain local Pharmacovigilance System Master Files (PSMFs) when required.
• Support the development and maintenance of local SOPs and agreements.
• Review and update Safety Data Exchange Agreements (SDEAs), Pharmacovigilance Agreements (PVAs), and Technical Agreements.
• Participate in audits, inspections, and the implementation of corrective actions.
• Ensure compliance with confidentiality, data privacy, and quality standards.

Required Qualifications

Education

• Bachelor's or Master's degree in Pharmacy, Medicine, Nursing, Life Sciences, or a related scientific discipline.
• Equivalent professional experience may also be considered.

Experience

• Minimum 2 years of experience in Pharmacovigilance.
• Experience in local PV case management, including case receipt, translation, submission, and follow-up.
• Strong knowledge of French and international pharmacovigilance regulations.
• Experience acting as a local pharmacovigilance contact in France is highly desirable.
• Previous experience in literature monitoring and regulatory intelligence is an advantage.
• Experience managing client interactions and projects is desirable.

Languages

• French: Native or fluent (written and spoken).
• English: Fluent (written and spoken).

Technical Skills

• Strong organizational and planning skills.
• Excellent attention to detail and quality mindset.
• Ability to work independently and manage priorities effectively.
• Strong interpersonal and communication skills.
• Good knowledge of Microsoft Office (Word, Excel, Outlook).
• Experience with safety databases and MedDRA is considered an advantage.

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Ready to take the next step? Apply today and join a global, innovative team that’s shaping the future of life sciences and empowering people to make a real impact in healthcare.

An international career, built around you

PLG partners with Life Sciences innovators to bring new medicines and technologies to patients, faster. Join a fast-growing, entrepreneurial company where your expertise makes a difference from day one.

Why PLG is the place to work

• A path for every career stage, from graduate to senior expert
• Exciting, high-impact projects with leading life sciences clients
• International by design
• Hybrid & flexible working
• Continuous learning
• An inclusive & diverse culture