Responsable Affaires Réglementaires

Working with Us
Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms the lives of patients and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits services and programs that provide our employees with the resources to pursue their goals both at work and in their personal lives. Read more: à Durée Déterminée à compter de mi-février 2026.

Rattaché au Directeur Adjoint Affaires Réglementaires vous réaliserez les activités liées aux missions du Département Affaires Règlementaires enFrance dans le respect des dispositions du Code de la Santé Publique des lois françaises et internationales de la Charte de linformation promotionnelle et des procédures internes en vigueur.

Plus précisément vous interviendrez sur:

• La publicité; vous vérifierez et approuverez les documents promotionnels et les supports de formation de la visite médicale en conformité avec la réglementation et vous vous assurerez du dépôt des dossiers de demande de visa publicité dans les délais requis. Notamment dans le cadre de lancement de produits.
• La pharmacovigilance et la gestion des risques; vous préparerez et mettrez à jour les outils de minimisation des risques des produits dont vous aurez la charge. Vous collaborerez également avec les équipes de Pharmacovigilance Internes ces produits.
• Vous serez également impliqué dans le suivi delenregistrement des produits en collaboration avec les équipes internationales la validation des articles de conditionnement et les constitutions des dossiers de transparence.
• Selon le développement du médicament vous serez impliqué dans la mise en œuvre daccès dérogatoires
• Vous serez amené à contribuer à desprojets transverses au sein du département.
• Vous fournirez un support et des conseils aux équipes concernées (marketing médical ventes et formations)
• Vous assurerez un support réglementaire auprès de la Direction Internationale des Affaires Réglementaires pour lautorisation et le suivi des essais cliniques mise en œuvre par BMS ou en collaboration avec des promoteurs institutionnels.

Profil et compétences recherchés :

• Pharmacien spécialisation en Affaires Réglementaires
• Au moins 1 ans dexpérience réussie en Affaires Réglementaires de préférence au sein de laboratoires de produits innovants.
• Esprit déquipe et aisance à travailler en équipe
• Rigueur et capacité danalyse
• Esprit positif et constructif solution-oriented
• Capacités dadaptation
• Anglais professionnel
• Maîtrise du pack Microsoft Office

Contexte: remplacement congés maternité (environ 6 mois)

If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position please visit this page for important additional information: Protection

We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R: Responsable Affaires Réglementaires