At a Glance
- Tasks: Manage regulatory submissions and health authority interactions for UK and Ireland.
- Company: Join a rapidly growing consultancy serving top multinational pharmaceutical companies.
- Benefits: Enjoy a part-time, fully remote role outside IR35 with flexible hours.
- Other info: This is a 12-month contract, perfect for those looking to balance work and studies.
- Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: Must have strong UK and Ireland regulatory experience, especially post-Brexit IRP knowledge.
The predicted salary is between 36000 - 60000 € per year.
Regulatory Affairs Manager - UK and Ireland outside IR35, part-time, remote
Your new companyThis rapidly growing Regulatory Affairs consultancy is looking for an experienced Regulatory Affairs Manager who specialises in UK and Ireland registrations to fulfil a 12-month, remote contract which is outside IR35.They count some of the biggest multinational pharmaceutical companies as clients and contin...
Regulatory Affairs Consultant Uk and Ire outside IR35 in Bedford employer: Hays
Join a dynamic and rapidly growing Regulatory Affairs consultancy that offers the flexibility of a part-time, fully remote role, allowing you to balance your professional and personal life. With a strong focus on employee growth and development, this company provides opportunities to work with leading multinational pharmaceutical clients while navigating the evolving regulatory landscape in the UK and Ireland. Experience a supportive work culture that values expertise and encourages collaboration, making it an excellent choice for those seeking meaningful and rewarding employment.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs Consultant Uk and Ire outside IR35 in Bedford
✨Tip Number 1
Familiarise yourself with the latest regulations and guidelines from the MHRA and HPRA. Being up-to-date will not only boost your confidence during discussions but also demonstrate your commitment to staying informed in this fast-paced field.
✨Tip Number 2
Network with professionals in the Regulatory Affairs sector, especially those who have experience with post-Brexit regulations. Engaging in conversations can provide insights and potentially lead to referrals that could enhance your application.
✨Tip Number 3
Prepare to discuss specific examples of your past experiences with regulatory submissions and health authority interactions. Highlighting your direct involvement in successful projects will showcase your expertise and readiness for the role.
✨Tip Number 4
Demonstrate your ability to work collaboratively with internal teams by sharing examples of how you've successfully implemented labelling changes in previous roles. This will show that you can effectively coordinate and communicate within a team setting.
We think you need these skills to ace Regulatory Affairs Consultant Uk and Ire outside IR35 in Bedford
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in regulatory affairs, particularly with UK and Ireland registrations. Emphasise any relevant post-Brexit experience and specific projects you've worked on that align with the job description.
Craft a Compelling Cover Letter:Write a cover letter that directly addresses the requirements of the role. Mention your familiarity with MHRA and HPRA submissions, and how your skills can contribute to the consultancy's success. Be sure to convey your enthusiasm for the position.
Showcase Relevant Skills:In your application, highlight key skills such as regulatory submissions, health authority interactions, and labelling management. Use specific examples to demonstrate your expertise and how you have successfully navigated similar challenges in the past.
Proofread Your Application:Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in regulatory affairs.
How to prepare for a job interview at Hays
✨Showcase Your Regulatory Expertise
Make sure to highlight your experience with UK and Ireland regulatory submissions, especially your familiarity with the MHRA and HPRA processes. Be prepared to discuss specific examples of past submissions and how you managed post-submission queries.
✨Demonstrate Your Knowledge of Recent Changes
Stay updated on recent regulatory changes post-Brexit, particularly regarding the International Recognition Procedure (IRP). Discuss how these changes impact the industry and be ready to explain how you would adapt to them in your role.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills in regulatory affairs. Think about challenges you've faced in previous roles and how you successfully navigated them, particularly in labelling and product information management.
✨Emphasise Collaboration Skills
Since the role involves working closely with internal teams, be sure to highlight your collaboration skills. Share examples of how you've effectively communicated and coordinated with different departments to implement regulatory changes.
