Senior Regulatory Affairs Associate - Maternity Cover

TN United Kingdom; London; On-site; GBP 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a Senior Regulatory Affairs Associate to oversee regulatory activities for store brand products in the UK. This role involves managing licensing, post-marketing submissions, and collaborating with retailers. The ideal candidate will have at least three years of experience in Regulatory Affairs, particularly with OTC medicines, and must demonstrate strong problem-solving and communication skills. Join a company that values its employees and offers competitive compensation along with career development opportunities.

Benefits

Competitive Compensation

Career Development Opportunities

Family Support Benefits

Qualifications

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

Responsibilities

• Handle licensing and post-marketing activities for store brand products.
• Manage submissions such as national variations and renewals.

Skills

Regulatory Affairs

OTC Medicines

Project Management

Communication Skills

Problem-Solving

Tools

TrackWise

eCTD Publishing Tools

Job description

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Senior Regulatory Affairs Associate - Maternity Cover, 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:

4483600654e7

Job Views:

2

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

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 store brand product within the Perrigo UKIE business.

Scope of the Role

In this role, you will handle licensing and post-marketing activities for store brand products marketed in the UK, focusing on collaboration with retailers and their own label designs.

• Main duties include:
• Exposure within UK regulatory framework for OTC medicines
• Coordinating artwork updates for variations submissions and liaising with other functions for implementation.
• Managing submissions such as national variations (Change Controls), renewals, safety updates, and change of ownership.
• Coordinating redesign updates with our artwork team and retailers
• Overseeing projects, monitoring compliance issues, and ensuring prompt resolution of urgent issues in collaboration with stakeholders.

Experience Required

Minimum of 3 years’ experience in Regulatory Affairs with OTC medicines, including Post Marketing License activities, renewals, and safety updates. Familiarity with CC-systems (e.g., TrackWise) and eCTD publishing tools is necessary. The ideal candidate should be:

• Self-motivated, flexible, and adaptable to changing requirements
• Highly driven and capable of working under pressure
• Autonomous and team-oriented
• Capable of supporting multiple activities concurrently
• Excellent communication skills in English
• Strong problem-solving skills
• Thorough, detail-oriented, and focused

We value our people highly. Alongside competitive compensation, we offer benefits supporting you and your family, as well as career development opportunities. Find out more about Perrigo. We are proud to be included in Forbes' "America's Best Employers by State 2024" list.

Applicants please note: To apply, click the APPLY button at the bottom of the application. The SAVE button only saves your profile, not your application. We are an equal opportunity employer, considering all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected characteristics. Our full EEO and Affirmative Action Policy is available on our career site in English and Spanish, and accessible formats for persons with disabilities.