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- Tasks: Lead regulatory activities for innovative drug launches in the UK and Ireland.
- Company: Join a dynamic pharmaceutical company focused on groundbreaking therapies.
- Benefits: Enjoy a collaborative work environment with opportunities for professional growth.
- Why this job: Be at the forefront of healthcare innovation and make a real impact.
- Qualifications: 5+ years in regulatory affairs with strong UK regulatory knowledge required.
- Other info: This role requires an EU work permit.
The predicted salary is between 43200 - 72000 £ per year.
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.
Regulatory Affairs Manager employer: JR United Kingdom
Contact Detail:
JR United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who work in regulatory affairs. Attend industry conferences or webinars to meet potential colleagues and learn about the latest trends and challenges in the field.
✨Tip Number 2
Stay updated on UK regulatory changes and guidelines by following relevant regulatory bodies and publications. This knowledge will not only enhance your expertise but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Consider reaching out to current or former employees of the company to gain insights into their experiences and the company culture. This can help you tailor your approach and show genuine interest in the position.
✨Tip Number 4
Prepare for potential interviews by practising answers to common regulatory affairs questions, particularly those related to pharmacovigilance and compliance. Being well-prepared will boost your confidence and help you stand out as a candidate.
We think you need these skills to ace Regulatory Affairs Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs, particularly within the pharmaceutical industry. Emphasise your knowledge of UK regulatory processes and any successful submissions or product launches you've been involved in.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the key responsibilities mentioned in the job description. Explain how your background aligns with their needs, particularly your experience as a Local Person for Pharmacovigilance and your ability to manage multiple priorities.
Showcase Relevant Experience: In your application, provide specific examples of your past work that demonstrate your expertise in regulatory affairs. Highlight any direct interactions with regulatory authorities and your understanding of compliance with national drug legislation.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in regulatory affairs.
How to prepare for a job interview at JR United Kingdom
✨Know Your Regulations
Make sure you have a solid understanding of UK regulatory processes and national drug legislation. Brush up on recent changes and be prepared to discuss how they might impact the company’s operations.
✨Showcase Your Experience
Be ready to share specific examples from your past roles that demonstrate your expertise in regulatory affairs. Highlight successful submissions and product launches to illustrate your capabilities.
✨Communicate Clearly
Strong communication skills are essential for this role. Practice articulating complex regulatory concepts in a clear and concise manner, as you may need to explain these to non-experts during the interview.
✨Prepare Questions
Think of insightful questions to ask about the company's upcoming drug launches and their regulatory strategies. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
