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- Tasks: Manage regulatory applications and ensure compliance with local regulations in a fast-paced environment.
- Company: Join a rapidly growing consultancy serving top multinational pharmaceutical companies.
- Benefits: Enjoy a part-time, fully remote role with flexible hours, outside IR35.
- Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: Strong background in UK and Ireland regulatory affairs is essential.
- Other info: This is a 12-month contract offering a unique opportunity to work remotely.
This rapidly growing Regulatory Affairs consultancy is looking for an experienced Regulatory Affairs Manager who specialises in UK and Ire registrations to fulfil a 12-month, remote contract which is outside IR35. They count some of the biggest multinational pharmaceutical companies as clients and continue to provide regulatory solutions that drive success.
As Regulatory Affairs Manager UK and Ire you will be responsible for:
- Submitting regulatory applications to local Health Authorities
- Ensuring compliance with local regulations when updating the Summary of Product Characteristics (SmPC) and Patient Information Leaflet (PIL)
- Handling Health Authority queries post-submission
This is a fast-paced, busy team, and we are looking for someone with a strong UK and Ire Regulatory background who can hit the ground running.
This is a part-time contract job, 21 – 28 hours per week. It is fully remote and outside IR35.
For more information on this Regulatory Affairs Manager UK and Ire job please apply.
Regulatory Affairs Specialist UK and Ireland, Part time, outside IR35 employer: Hays
Contact Detail:
Hays Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Specialist UK and Ireland, Part time, outside IR35
✨Tip Number 1
Network with professionals in the regulatory affairs field, especially those who have experience with UK and Ireland regulations. Attend industry events or webinars to connect with potential colleagues and learn about the latest trends.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements for pharmaceutical products in the UK and Ireland. This knowledge will not only boost your confidence but also demonstrate your expertise during any discussions with the hiring team.
✨Tip Number 3
Prepare to discuss your previous experiences with regulatory submissions and compliance. Be ready to share specific examples of how you've successfully navigated challenges in this area, as it will show your capability to hit the ground running.
✨Tip Number 4
Research the consultancy's clients and their products. Understanding their portfolio will help you tailor your conversations and show that you're genuinely interested in contributing to their success.
We think you need these skills to ace Regulatory Affairs Specialist UK and Ireland, Part time, outside IR35
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the specific responsibilities and requirements for the Regulatory Affairs Specialist position. Tailor your application to highlight your relevant experience in UK and Ireland regulatory affairs.
Highlight Relevant Experience: In your CV and cover letter, emphasise your previous roles related to regulatory submissions and compliance. Provide specific examples of how you've successfully managed applications and handled queries from Health Authorities.
Showcase Your Skills: Make sure to include key skills that are relevant to the role, such as attention to detail, knowledge of local regulations, and the ability to work in a fast-paced environment. Use bullet points for clarity.
Craft a Compelling Cover Letter: Write a personalised cover letter that explains why you are interested in this part-time role and how your background makes you a perfect fit. Mention your understanding of the consultancy's client base and your enthusiasm for contributing to their success.
How to prepare for a job interview at Hays
✨Know Your Regulations
Make sure you have a solid understanding of the UK and Ireland regulatory landscape. Brush up on the latest guidelines and requirements for submitting applications to local Health Authorities, as this will demonstrate your expertise and readiness for the role.
✨Prepare for Scenario Questions
Expect questions that assess how you would handle specific regulatory challenges or queries from Health Authorities. Think of examples from your past experience where you successfully navigated similar situations, as this will showcase your problem-solving skills.
✨Highlight Your Experience
Be ready to discuss your previous roles in regulatory affairs, particularly any experience with multinational pharmaceutical companies. Emphasise your ability to manage compliance and update documents like the Summary of Product Characteristics (SmPC) and Patient Information Leaflet (PIL).
✨Show Your Adaptability
Since this is a part-time, remote position, highlight your ability to work independently and manage your time effectively. Discuss any previous remote work experiences and how you maintained productivity and communication with your team.
