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- Tasks: Lead the Regulatory Affairs team and ensure compliance with MHRA regulations.
- Company: Join a dynamic specialty pharmaceutical distribution company in Greater Manchester.
- Benefits: Enjoy a hybrid work model with a minimum of 3 days onsite each week.
- Why this job: Step into a senior leadership role and make a real impact in the pharmaceutical industry.
- Qualifications: 5+ years in Regulatory Affairs with proven MHRA experience required.
- Other info: This is a permanent, full-time position; applicants must have valid Right to Work in the UK.
The predicted salary is between 48000 - 84000 £ per year.
1 week ago Be among the first 25 applicants Direct message the job poster from Blackfield Associates Senior International Consultant – Regulatory Affairs and Executive Search Blackfield are supporting a specialty pharmaceutical distribution company, based in Greater Manchester, hiring for a Senior Regulatory Affairs Manager. This is a great opportunity for an experienced Regulatory professional to step up into senior leadership. As Head of Regulatory Affairs, you will: Lead the Regulatory Affairs team Oversight of license compliance with MHRA Submit new MAA / licenses variations to regulatory authority Act as point of contact for the company with the MHRA, external stakeholders and license users Assist in the training and further development of junior RA team members Managing approved suppliers for repackaging To be considered for the role of Head of Regulatory Affairs, you will have: Minimum 5 years experience in Regulatory Affairs, ideally gained in a generic, specialty or pharma distribution Must have proven MHRA experience, including submissions and acting as point of contact/ lead meetings Strong cGMP, gained within wholesale distribution or drug manufacturing Previous line management/ leading a team A strong communicator, looking to develop their career and be a leader This is a permanent position, working hybrid from our client\’s Greater Manchester base. Minimum 3 days per week onsite. Unable to sponsor, all applicants must hold valid Right to Work in the UK. Seniority level Mid-Senior level Employment type Full-time Job function Distribution and Quality Assurance Industries Pharmaceutical Manufacturing and Retail Pharmacies #J-18808-Ljbffr
Senior Manager Regulatory Affairs employer: Blackfield Associates
Contact Detail:
Blackfield Associates Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager Regulatory Affairs
✨Tip Number 1
Network with professionals in the Regulatory Affairs field, especially those who have experience with the MHRA. Attend industry events or webinars to connect with potential colleagues and learn about the latest trends in regulatory compliance.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines set by the MHRA. Being well-versed in these can help you demonstrate your expertise during interviews and discussions with the hiring team.
✨Tip Number 3
Prepare to discuss your leadership experience in detail. Think of examples where you've successfully managed a team or led projects, as this role requires strong management skills and the ability to mentor junior team members.
✨Tip Number 4
Research the company’s recent activities and any news related to their regulatory affairs. This knowledge will not only help you tailor your conversations but also show your genuine interest in the role and the organisation.
We think you need these skills to ace Senior Manager Regulatory Affairs
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in Regulatory Affairs, especially your work with the MHRA and any leadership roles you've held. Use specific examples to demonstrate your achievements and skills.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role. Mention how your background aligns with the responsibilities of leading a Regulatory Affairs team and your commitment to compliance.
Highlight Relevant Experience: In your application, emphasise your minimum 5 years of experience in Regulatory Affairs, particularly in generic or specialty pharmaceuticals. Detail your proven track record with submissions and your role as a point of contact for regulatory authorities.
Showcase Leadership Skills: Since this role involves managing a team, be sure to include examples of your previous line management experience. Discuss how you have trained and developed junior team members, showcasing your ability to lead and inspire.
How to prepare for a job interview at Blackfield Associates
✨Showcase Your Regulatory Expertise
Make sure to highlight your experience in Regulatory Affairs, especially your work with the MHRA. Be prepared to discuss specific submissions you've managed and how you navigated any challenges.
✨Demonstrate Leadership Skills
As this role involves leading a team, be ready to share examples of your previous leadership experiences. Discuss how you've developed junior team members and managed projects effectively.
✨Communicate Clearly and Confidently
Strong communication is key for this position. Practice articulating your thoughts clearly, especially when discussing complex regulatory topics. This will show your ability to be a point of contact for stakeholders.
✨Prepare Questions for the Interviewers
Have insightful questions ready about the company's regulatory strategies and team dynamics. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
