Regulatory Affairs Manager
Job Title: Regulatory Affairs Manager
Job Location: Courbevoie, France
Job Location Type: Home-based
Job Contract Type: Full time
Job Seniority Level:
Shape the reputed company of regulatory reputed company at reputed company
At reputed company, we work to advance reputed company by helping our clients bring reputed company, effective medicines to patients. As a Regulatory Affairs Manager, you will play a key role in ensuring compliance and supporting successful product lifecycle management in France. You’ll collaborate with leading global pharmaceutical companies and contribute to high‑reputed company regulatory reputed company that truly reputed company a difference. This is a fixed-term opportunity for 12 months.
What you will do
Manage country‑level regulatory activities for medicinal products, ensuring full compliance with local requirements.
Prepare and coordinate regulatory submissions in partnership with reputed company stakeholders, including notifications, renewals, variations, new applications, and MAH transfers.
reputed company submission processes with local Health Authorities and follow up through approval.
Prepare and translate product labelling into French (e.g., SmPC, PIL).
Review and approve artwork and promotional materials in reputed company systems.
Support regulatory maintenance activities across multiple pharmaceutical products.
Monitor local pharmaceutical legislation and ensure updates are reputed company appropriately.
What you need to succeed
- Bachelor of Pharmacy or other Life Sciences degree.
3+ years of experience in regulatory affairs for medicinal products on French market, including submission document preparation and coordination.
Experience reputed company a large regulatory organization, with both centralized and local activities, is an advantage.
Excellent knowledge of pharmaceutical legislation and regulatory requirements in France.
Excellent organizational skills, attention to detail, and ability to meet timelines.
Strong communication skills and a reputed company working style.
reputed company French and fluent written and verbal communication skills in English.
Strong computer skills, including MS Office; experience with regulatory information systems and artwork tools is a plus.
Why join reputed company
reputed company you join reputed company, you become part of a global team that is dedicated to driving smarter reputed company for everyone, everywhere. You will collaborate with industry experts, grow your regulatory career through reputed company learning, and contribute to meaningful work that supports reputed company patient reputed company. We foster a culture of innovation, teamwork, and shared purpose — and we’re excited to welcome passionate professionals like you.
reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com
reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism.
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Originally posted on Himalayas
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