Regulatory Affairs - Senior Associate

TN United Kingdom; London; Hybrid; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Senior Regulatory Affairs Associate to join their dynamic team in London. In this pivotal role, you will manage regulatory activities for a portfolio of branded products, ensuring compliance with legislation while supporting product development. The company fosters a collaborative culture, promoting flexibility with a hybrid working approach. You will have the opportunity to work autonomously and as part of a multi-functional team, contributing to the health and wellness solutions that improve lives. If you are driven and detail-oriented, this is the perfect opportunity for you.

Benefits

Flexible Working Hours

Career Development Opportunities

Competitive Compensation

Health and Wellness Benefits

Remote Work Options

Qualifications

• Minimum 3 years’ experience in Regulatory Affairs with OTC medicines.
• Familiarity with CC-systems and eCTD publishing tools.

Responsibilities

• Provide regulatory input to new product development and documentation.
• Communicate with local regulatory authorities regarding license applications.
• Ensure product registrations are compliant with relevant legislation.

Skills

Regulatory Affairs

OTC Medicines

Problem-Solving

Attention to Detail

Project Management

Education

Bachelor's Degree in Life Sciences

Regulatory Affairs Certification

Tools

TrackWise

eCTD Publishing Tools

Job description

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Regulatory Affairs - Senior Associate, London

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Client:

Perrigo

Location:

London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

0d0375485b48

Job Views:

6

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

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.

Find out more aboutTotal Rewardsat Perrigo.

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