Assistant - Regulatory Affairs Lifecycle Management Medicines

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®, 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 win in self-care.

Description Overview

We are excited to recruit an Assistant Professional Regulatory Affairs- Medicines Lifecycle Management to our team. You will support Perrigo's medicinal product portfolio throughout the product lifecycle, contributing to regulatory activities that help maintain product compliance, marketing authorisations, availability and market access across multiple markets.

You will assist with lifecycle management activities, including the preparation, submission and maintenance of regulatory submissions, marketing authorisation dossiers and related regulatory documentation in line with applicable regulatory requirements and business priorities. Working as part of a Regulatory Affairs team, you will support the delivery of submissions and help ensure regulatory records are accurate, current and compliant.

You will support a range of regulatory activities, including product maintenance, change management and ongoing compliance obligations. Through close collaboration with colleagues, you will help identify and address regulatory issues, contribute to risk mitigation activities and support the delivery of regulatory objectives.

Working with cross-functional stakeholders including Quality, Safety, Supply Chain, Manufacturing and R&D, you will provide regulatory support for product and process changes and assist in implementing regulatory requirements that support compliance and business needs.

You will contribute to the continuous improvement of Regulatory Affairs processes, systems and ways of working, helping to improve efficiency, consistency and quality across lifecycle activities. Through your role, you will develop foundational knowledge of medicinal product regulations and gain experience working within a global regulatory environment.

This role offers an excellent opportunity to begin or further develop a career in Medicines Regulatory Affairs, building technical expertise, regulatory knowledge and professional capabilities while supporting Perrigo's commitment to maintaining high standards of compliance, patient safety and product quality

Scope of the Role

• Supports the compliant maintenance of Perrigo’s portfolio by contributing to post-approval regulatory activities, documentation quality, and implementation tracking across products and markets.
• Provides an entry point into Regulatory Affairs for either a graduate building foundational regulatory capability or an experienced administrator/coordinator moving into a regulatory career pathway.
• Builds practical understanding of lifecycle delivery while operating with agility across changing priorities and supporting a flexible work remit in line with business needs.
• Supports post-launch regulatory execution within Lifecycle Management under the direction of more experienced regulatory colleagues.
• Works across regulatory change documentation, trackers, and basic implementation support for defined products or workstreams.
• Contributes within project teams with no people leadership and increasing exposure to product types, markets, and regulatory systems.

Lifecycle Delivery Support

• Support preparation, compilation, and maintenance of lifecycle regulatory documentation, dossiers, and trackers.
• Assist with submission planning and tracking for post-approval variations/changes, renewals, notifications, and related maintenance activities.
• Gather and organise source information required to support regulatory assessments, documentation updates, and implementation activities.
• Contribute to accurate implementation tracking for approved changes to help protect compliance and continuity of supply.

Compliance, Documentation & Process Discipline

• Maintain records and documentation in line with Good Documentation Practice and established regulatory and quality processes.
• Support responses to routine internal or external regulatory queries under guidance.
• Escalate uncertainties, gaps, or risks promptly and accurately.
• Contribute to disciplined handover and transition of regulatory information, decisions, and files across interfaces.

Learning, Collaboration & Ways of Working

• Build understanding of lifecycle processes, regulatory requirements, systems, and terminology across products and markets.
• Work effectively with Lifecycle Management, Category, Cluster, Quality, Safety, R&D, Supply, Artwork, and Regulatory Operations colleagues.
• Demonstrate flexibility to support a range of administrative, coordination, and entry-level regulatory activities depending on business priorities.

Experience Required

• Degree in Life Sciences or a related discipline, or relevant administrative/co-ordination experience in a regulated, quality-driven, or document-intensive environment.
• Entry level role for people with up to 2 years Regulatory Affairs experience, preferably within medicinal products or another regulated healthcare product area.
• Strong organisational skills, attention to detail, and the ability to manage information accurately in a structured environment.
• Demonstrated ability to work collaboratively and learn quickly.

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 about at 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 more

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.) All application materials, including resumes and CVs, must be submitted in English. 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