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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 part of exciting drug launches and make a real impact in healthcare.
- 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
Prepare for potential interviews by practising answers to common regulatory affairs questions. Focus on your experience with successful submissions and product launches, as these are key aspects of the role.
✨Tip Number 4
Consider reaching out to current or former employees of the company to gain insights into their culture and expectations. This can help you tailor your approach and show that you’re genuinely interested in joining their team.
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: In your cover letter, explain why you are passionate about regulatory affairs and how your background aligns with the company's mission. Mention specific experiences that demonstrate your expertise and ability to manage regulatory activities effectively.
Highlight Relevant Skills: Clearly outline your strong communication and organisational skills in your application. Provide examples of how you've successfully managed multiple priorities in a fast-paced environment, as this is crucial for the role.
Showcase Continuous Learning: Mention any recent training or certifications related to regulatory affairs or pharmacovigilance. This shows your commitment to staying updated with the latest regulatory requirements and enhances your application.
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.
✨Demonstrate Adaptability
The pharmaceutical industry is fast-paced and ever-changing. Be prepared to discuss how you've successfully managed multiple priorities and adapted to new challenges in your previous positions.
