Regulatory Affairs Manager

JR United Kingdom; United Kingdom; On-site; GBP 50,000 - 80,000; Full time

Job summary

An innovative pharmaceutical company is seeking a Regulatory Affairs Manager for the UK and Ireland. In this pivotal role, you will provide expert regulatory guidance, manage regulatory activities, and ensure compliance with UK regulations. With several exciting drug launches on the horizon, this position offers a unique opportunity to contribute to groundbreaking therapies. Join a dynamic team where your expertise will help shape the future of healthcare. If you thrive in fast-paced environments and have a passion for regulatory affairs, this is the role for you!

Qualifications

• 5+ years in regulatory affairs within the pharmaceutical industry.
• Expert knowledge of UK regulatory processes.

Responsibilities

• Provide UK regulatory expertise to the organization.
• Manage regulatory activities for the UK and Ireland.

Skills

Regulatory Affairs Expertise

Communication Skills

Organizational Skills

Knowledge of UK Drug Legislation

Education

Bachelor's Degree in Life Sciences

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 innovative 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.