Local Safety Officer

ProductLife Group; Courbevoie; On-site; EUR 60,000 - 90,000; Full time

Job summary

ProductLife Group seeks a Local Safety Officer to support pharmacovigilance activities in France, acting as a local expert and key contact for French authorities. You will ensure compliance with local and international PV requirements and collaborate with clients and internal teams.

The role requires strong PV knowledge, local case management experience, and excellent communication skills to interact with health authorities, clients, and stakeholders.

Qualifications

• Bachelor's or Master's degree in Pharmacy, Medicine, Life Sciences, or related field.
• Minimum 2 years of Pharmacovigilance experience.
• Fluent in French and English.

Responsibilities

• Act as Local Safety Officer for PLG clients in France.
• Liaise with French regulatory authorities on pharmacovigilance matters.
• Support Local Pharmacovigilance Person (LPPV) responsibilities.
• Ensure local vigilance activities and regulatory compliance.
• Monitor and interpret local pharmacovigilance regulations.
• Prepare and/or support safety submissions when required.
• Coordinate communication with clients and authorities within agreed timelines.

Skills

Pharmacovigilance

Local PV contact

Case management

Regulatory liaison

Documentation

Education

Bachelor's or Master's in Pharmacy/Medicine/Life Sciences

Tools

MedDRA

MS Office

Job description

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.

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.