Regulatory Affairs Manager

JR United Kingdom; High Wycombe; On-site; GBP 40,000 - 65,000; Full time

Job summary

A leading pharmaceutical company is seeking a Regulatory Affairs Manager to oversee regulatory compliance and manage activities in the UK and Ireland. The role involves working closely with regulatory authorities and supporting the launch of innovative drugs. Candidates should have at least 5 years of regulatory experience and a proven track record of success in submissions and launches.

Qualifications

• Minimum of 5 years of experience in regulatory affairs within the pharmaceutical industry.
• Expert knowledge of UK regulatory processes and national drug legislation.
• Ability to manage multiple priorities in a fast-paced environment.

Responsibilities

• Provide UK regulatory expertise and manage regulatory activities for the UK and Ireland.
• Ensure compliance with UK regulatory processes and national drug legislation.
• Liaise with regulatory authorities for successful product launches.

Skills

Communication

Organizational skills

Regulatory knowledge

Job description

Social network you want to login/join with:

Regulatory Affairs Manager, high wycombe

col-narrow-left

Client:

Location:

high wycombe, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

9

Posted:

06.06.2025

Expiry Date:

21.07.2025

col-wide

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.