Regulatory Affairs Manager

JR United Kingdom; Shrewsbury; On-site; GBP 60,000 - 80,000; Full time

Job summary

Une entreprise pharmaceutique dynamique et innovante recherche un Responsable des Affaires Réglementaires pour le Royaume-Uni et l'Irlande. Ce rôle implique de fournir des conseils réglementaires essentiels, de gérer les activités réglementaires et de soutenir les lancements de nouveaux médicaments innovants. Plusieurs lancements passionnants sont prévus dans les prochaines années, offrant ainsi une belle opportunité de développement professionnel.

Qualifications

• Minimum 5 ans d'expérience en affaires réglementaires dans l'industrie pharmaceutique.
• Connaissance approfondie des processus réglementaires britanniques.
• Capacité à gérer plusieurs priorités dans un environnement rapide.

Responsibilities

• Fournir une expertise réglementaire pour le Royaume-Uni.
• Gérer les activités réglementaires pour le Royaume-Uni et l'Irlande.
• Assurer la conformité avec les processus réglementaires du Royaume-Uni.

Skills

Expertise réglementaire

Compétences en communication

Organisation

Job description

Social network you want to login/join with:

Regulatory Affairs Manager - Pharmaceuticals

As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. Additionally, you will serve as the Local Person for Pharmacovigilance (LPPV) and the National Pharmacovigilance Contact Person.

We are a dynamic and innovation pharmaceutical company, dedicated to bringing groundbreaking therapies to markets. With several exciting drug launches planned over the next 24 months, we are looking for a dedicated and experienced Regulatory Affairs Manager to join our team.

Key Responsibilities:

• Provide UK regulatory expertise to the organization.
• Manage regulatory activities for the UK and Ireland.
• Serve as the LPPV/National Pharmacovigilance Contact Person.
• Ensure compliance with UK regulatory processes and national drug legislation.
• Support the launch of innovative drugs over the coming years.
• Liaise with regulatory authorities and maintain up-to-date knowledge of regulatory requirements.

Qualifications:

• Minimum of 5 years of experience in regulatory affairs within the pharmaceutical industry.
• Expert knowledge of UK regulatory processes and national drug legislation.
• Strong communication and organizational skills.
• Ability to work in a fast-paced environment and manage multiple priorities.
• Proven track record of successful regulatory submissions and product launches.