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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.
The predicted salary is between 30000 - 42000 £ per year.
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 interviews.
✨Tip Number 3
Prepare to discuss real-life scenarios where you've successfully navigated regulatory challenges. Having concrete examples ready will showcase your problem-solving skills and ability to handle Health Authority queries effectively.
✨Tip Number 4
Stay updated on any changes in regulations or guidelines that affect the pharmaceutical industry in the UK and Ireland. Being knowledgeable about current events will help you stand out as a proactive candidate.
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 of 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, compliance with local regulations, and any experience with Health Authorities. Use specific examples to demonstrate your expertise.
Craft a Strong Cover Letter: Write a compelling cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role. Mention why you are interested in working with a consultancy that serves multinational pharmaceutical companies.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in regulatory affairs.
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 Communication Skills
As a Regulatory Affairs Manager, you'll need to communicate effectively with various stakeholders. Be prepared to discuss how you've managed communications in previous roles, especially when dealing with complex regulatory information or responding to queries.
✨Show Your Adaptability
This role is in a fast-paced environment, so be ready to talk about how you've adapted to changes in regulations or project demands in the past. Sharing examples of your flexibility and ability to work under pressure will make you stand out.
