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- Tasks: Manage regulatory projects and ensure compliance for medicinal products in the UK and Ireland.
- Company: Join Perrigo, a top player in the European Consumer Self-Care market.
- Benefits: Enjoy competitive pay, family support, and career development opportunities.
- Other info: Flexible hybrid working model with a collaborative and inclusive culture.
- Why this job: Make a real impact on health and wellness solutions that everyone trusts.
- Qualifications: Scientific degree and 3 years of Regulatory Affairs experience required.
The predicted salary is between 40000 - 50000 £ per year.
At Perrigo, we are driven by our mission to make lives better through trusted health and wellness solutions, accessible to all. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula. Dedicated to providing the best self-care for everyone, we are the people behind the brands you trust. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to win in self-care.
Description Overview
As a member of the Europe North Cluster Regulatory Affairs Team, the Senior Regulatory Affairs Associate will focus on post-marketing regulatory activities for medicinal products within the UK and Ireland. This role is a 6-month Fixed Term Contract.
Scope of the Role
- Work on Regulatory Affairs projects & product changes to meet business needs.
- Comply with the existing legislation and regulations for medicines.
- Ensure product registrations are correct and compliant with the relevant legislation.
- Establish, review, approve and update regulatory documentation.
- Prepare & submit variations via the electronic platforms.
- Maintain accurate and complete records by updating the relevant trackers, product folders and regulatory databases.
- Approve Artwork and Texts from a regulatory perspective.
- Participate in project meetings with both internal and external stakeholders.
- Communicate with local regulatory authorities regarding license applications and variations.
- Maintain oversight of the assigned projects, keep informed of any issues affecting product compliance or supply to market and take prompt action when urgent issues arise.
- Carry out other related regulatory affairs duties as required.
Experience Required
- A scientific degree in a pharmaceutical, chemical or biological discipline.
- 3 years Regulatory Affairs experience, ideally within UK or EU OTC including Post Marketing Licence Maintenance activities.
Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Hybrid Working Approach
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.
We are proud to be included in the Forbes list of 'America's Best Employers by State 2024'.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.
Senior Regulatory Affairs Associate - 6 Month Fixed Term Contract employer: Perrigo
Contact Detail:
Perrigo Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Affairs Associate - 6 Month Fixed Term Contract
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews by researching Perrigo and its products. Understand their mission and values, and think about how your experience aligns with their goals. We want to see that you’re genuinely interested in being part of the One Perrigo journey!
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources to get comfortable with common questions. We can’t stress enough how important it is to articulate your experience clearly and confidently.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows us that you’re serious about joining our team at Perrigo. Let’s make lives better together!
We think you need these skills to ace Senior Regulatory Affairs Associate - 6 Month Fixed Term Contract
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experience that match the Senior Regulatory Affairs Associate role. Highlight your regulatory affairs experience, especially in post-marketing activities, to show us you’re the right fit!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you’re passionate about regulatory affairs and how your background aligns with our mission at Perrigo. Keep it concise but impactful!
Showcase Relevant Experience: When filling out your application, be specific about your previous roles in regulatory affairs. Mention any projects you've worked on that relate to compliance and product registrations, as this will resonate with us.
Apply Through Our Website: Don’t forget to hit that APPLY button at the bottom of the application page! Applying through our website ensures your application gets to us directly, so we can review it promptly.
How to prepare for a job interview at Perrigo
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulations and guidelines related to medicinal products in the UK and Ireland. Being able to discuss specific legislation and how it impacts post-marketing activities will show that you're not just familiar with the role, but that you're genuinely passionate about regulatory affairs.
✨Showcase Your Project Management Skills
Since this role involves overseeing various regulatory projects, be prepared to share examples of how you've successfully managed similar tasks in the past. Highlight your ability to keep track of multiple projects, communicate with stakeholders, and take prompt action when issues arise.
✨Prepare for Scenario Questions
Expect questions that put you in hypothetical situations related to regulatory compliance or product changes. Think through how you would handle urgent issues or communicate with local authorities. This will demonstrate your problem-solving skills and your ability to think on your feet.
✨Emphasise Team Collaboration
Perrigo values an inclusive and collaborative culture, so be ready to discuss how you've worked effectively within a team. Share experiences where you’ve collaborated with internal and external stakeholders, and how you contributed to a positive team environment while achieving regulatory goals.