Regulatory Affairs Manager

JR United Kingdom; Crawley; On-site; GBP 55,000 - 75,000; Full time

Job summary

A leading pharmaceutical company seeks a Regulatory Affairs Manager for the UK and Ireland to provide regulatory guidance and oversee compliance activities. The role involves managing regulatory submissions and supporting the launch of innovative drugs, requiring extensive experience in the pharmaceutical industry.

Qualifications

• 5+ years of experience in regulatory affairs within the pharmaceutical industry.
• Expert knowledge of UK regulatory processes and legislation.
• Proven track record of successful regulatory submissions and product launches.

Responsibilities

• Provide UK regulatory expertise to the organization.
• Manage regulatory activities for the UK and Ireland.
• Liaise with regulatory authorities and ensure compliance.

Skills

Strong communication

Organizational skills

Ability to manage multiple priorities

Education

Minimum of 5 years in regulatory affairs

Job description

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Regulatory Affairs Manager, crawley, west sussex

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Client:

Location:

crawley, west sussex, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

9

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

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.