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- Tasks: Join our team as a Senior Regulatory Affairs Associate, managing product compliance and documentation.
- Company: Perrigo is a leading player in the European Consumer Self-Care market, dedicated to health and wellness.
- Benefits: Enjoy competitive pay, hybrid work options, and career development opportunities.
- Why this job: Be part of a collaborative culture that values inclusivity and personal growth while making a real impact.
- Qualifications: 3+ years in Regulatory Affairs with OTC medicines; detail-oriented and self-motivated.
- Other info: Work from our central London office with flexibility to work remotely two days a week.
The predicted salary is between 36000 - 60000 £ per year.
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At Perrigo, we are driven by our mission to Makes 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 Opill, Compeed, Solpadeine, NiQuitin, ACO, and many more. We Are Perrigo . 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 a blended-branded business to win in self-care.
Description Overview
We are hiring a talented Senior Regulatory Affairs Associate who will be responsible for the hands-on regulatory activities associated with maintaining the portfolio of branded products within the Perrigo UKIE business.
Our office is in central London.
Scope of the Role
- Work as part of a multi-functional team by providing regulatory input to new product development and associated supporting documentation, complete due diligence on time for any assigned product dossiers.
- As part of the team ensure product registrations are correct and compliant with the relevant legislation. Establish, review, approve and update regulatory documentation
- Prepare and publish packages and submit MAA’s and variations to meet the business needs 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 contacts
- Communicate with local regulatory authorities regarding license applications and variations
- Interpret and implement legislation, follow changes in national regulations and legislations and proactively manage impact of these changes
- Support marketing and sales with claims creation and copy review, as per internal guidelines
- Carry out other related regulatory affairs duties as required
Experience Required
Our ideal candidate should have a minimum of 3 years’ experience in Regulatory Affairs, working with OTC medicines, including Post Marketing License Maintenance activities, renewals and safety updates.
You should be familiar with working in CC-systems (e.g. TrackWise) and eCTD publishing tools.
The person we are looking for should be:
- Self-motivated, flexible and open to changing requirements
- Highly driven with enthusiasm to meet requirements and cope under demanding pressure
- The ability to work autonomously and in a team
- The ability to support several concurrent activities
- Excellent problem-solving skills
- Being thorough, focused and detail oriented
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\”. Find out morehere
Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
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Regulatory Affairs - Senior Associate employer: Perrigouk
Contact Detail:
Perrigouk Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs - Senior Associate
✨Tip Number 1
Familiarize yourself with the specific regulatory frameworks and guidelines relevant to OTC medicines in the UKIE market. This knowledge will not only help you during interviews but also demonstrate your commitment to understanding the industry.
✨Tip Number 2
Network with professionals in the Regulatory Affairs field, especially those who have experience with Perrigo or similar companies. Engaging in conversations can provide insights into the company culture and expectations, which can be beneficial during the application process.
✨Tip Number 3
Stay updated on recent changes in regulations and legislation affecting the self-care and OTC medicine sectors. Being able to discuss current trends and their implications during your interview will showcase your proactive approach and expertise.
✨Tip Number 4
Prepare to discuss specific examples from your past experience that highlight your problem-solving skills and ability to work under pressure. Tailoring your responses to reflect the responsibilities outlined in the job description will make you a standout candidate.
We think you need these skills to ace Regulatory Affairs - Senior Associate
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior Regulatory Affairs Associate position. Understand the key responsibilities and required experience, especially in OTC medicines and regulatory documentation.
Tailor Your CV: Customize your CV to highlight relevant experience in Regulatory Affairs, particularly focusing on your work with OTC medicines, post-marketing license maintenance, and any familiarity with CC-systems and eCTD publishing tools.
Craft a Strong Cover Letter: Write a compelling cover letter that reflects your enthusiasm for the role and Perrigo's mission. Mention specific experiences that demonstrate your problem-solving skills and ability to work under pressure.
Follow Application Instructions: Make sure to click the APPLY button at the bottom of the application page to submit your application. Remember, using the SAVE button will not submit your application, so double-check before you finalize your submission.
How to prepare for a job interview at Perrigouk
✨Understand Regulatory Frameworks
Make sure you have a solid grasp of the regulatory frameworks relevant to OTC medicines. Be prepared to discuss how you've navigated these regulations in your previous roles, especially regarding product registrations and compliance.
✨Showcase Your Experience
Highlight your experience in Regulatory Affairs, particularly with Post Marketing License Maintenance activities. Be ready to provide specific examples of how you've managed renewals and safety updates effectively.
✨Demonstrate Problem-Solving Skills
Prepare to discuss instances where you've encountered challenges in regulatory processes and how you resolved them. This will showcase your problem-solving abilities and attention to detail, which are crucial for this role.
✨Familiarize Yourself with Tools
Since familiarity with CC-systems like TrackWise and eCTD publishing tools is important, be ready to talk about your experience with these systems. If you have any specific achievements or efficiencies you've created using these tools, make sure to mention them.
