
Head Of Regulatory Affairs H/F Approach People Recruitment
Genève-Annemasse - 74 CDIOffre d’un cabinet de recrutement
-
Cette offre est publiée par un cabinet de recrutement. Il ne s'agit pas de l'entreprise dans laquelle vous travaillerez au quotidien.
- 80 000 - 150 000 € / an
- Bac +5
- Services aux Entreprises
- Exp. + 7 ans
Détail du poste
As the Head of Regulatory Affairs, you will BE responsible for overseeing and leading the regulatory affairs team for a company specializing in medical devices. You will work closely with the research and development, quality, manufacturing, marketing, and sales departments to ensure regulatory compliance for all products and processes.
Responsibilities :
- Manage and lead the regulatory affairs team, including activity planning, goal setting, and performance evaluation.
- Develop and implement regulatory strategies to ensure compliance with local and international standards.
- Ensure timely and effective submission of regulatory filings to relevant authorities, including new product approvals, renewals, and modifications.
- Evaluate regulatory requirements for new products and changes to existing products, providing strategic guidance to the product development team.
- Manage interactions with regulatory agencies and external partners, ensuring effective and positive relationships.
- Maintain constant regulatory surveillance to identify new requirements and potential regulatory developments impacting the company.
- Collaborate with internal teams to develop and implement regulatory compliance management processes and systems.
- Participate in internal and external audits related to regulatory affairs, ensuring appropriate corrective and preventive actions are implemented.
- Provide regulatory expertise and guidance to other departments within the company, including training on applicable regulatory requirements.
Your profil :
- University degree in life sciences, biomedical engineering, or a related field.
- At least 10 years experience in regulatory affairs, preferably in the medical devices sector.
- In-depth knowledge of local and international regulations related to medical devices, such as FDA, EMA, and European directives.
- Proven experience in team management and leadership.
- Excellent communication skills and demonstrated ability to work collaboratively with multifunctional teams.
- Ability to work independently, manage priorities, and meet tight deadlines.
- Proficiency in English and German, both spoken and written; proficiency in french would BE an advantage.
- Genève-Annemasse - 74
- CDI
Créez une alerte
Pour être informé rapidement des nouvelles offres, merci de préciser les critères :
Finalisez votre candidature
sur le site du recruteur
Créez votre compte pour postuler
sur le site du recruteur !
sur le site du recruteur
sur le site du recruteur !
Ces offres pourraient aussi
vous intéresser



Recherches similaires
- Emploi Chargé d'affaires réglementaires
- Emploi Qualité
- Emploi Annecy
- Emploi Annemasse
- Emploi Sallanches
- Emploi Thonon-les-Bains
- Emploi Rumilly
- Emploi Cluses
- Emploi Seyssel
- Emploi La Roche-sur-Foron
- Emploi Évian-les-Bains
- Emploi Saint-Julien-en-Genevois
- Emploi Technicien de qualité
- Emploi Responsable qualité
- Emploi Contrôleur de qualité
- Emploi Responsable QSE
- Emploi Assistant qualité
- Entreprises Qualité
- Entreprises Chargé d'affaires réglementaires
- Entreprises Genève-Annemasse
- Emploi Senior
- Emploi Montagne
- Emploi Expert
- Emploi Biomedical
- Emploi Local
{{title}}
{{message}}
{{linkLabel}}