Professional Regulatory Affairs - Lifecycle Management - Non-Medicines

Description Overview

We are excited to recruit a Regulatory Affairs Professional within Non-Medicinal Lifecycle Management. You will play an important role in supporting Perrigo's non-medicinal portfolio including cosmetics, VMS, general products, and other non-medicinal classifications such as medical devices across the product lifecycle.

Scope of the Role

• Ensures regulatory compliance of assigned products through independent ownership of lifecycle regulatory activities across multiple products and markets.
• Takes ownership of post-market lifecycle changes, regulatory filings, documentation updates, and regulatory issues of moderate to significant complexity, translating requirements into practical, risk-based execution.
• Contributes to both executional and strategic aspects of lifecycle projects and begins to lead workstreams within the LCM remit.
• Independently manages a range of complex product lifecycle changes, regulatory filings, notifications, registrations, and documentation updates across products and markets.
• Works mostly independently end-to-end, seeking alignment for high-risk decisions and providing risk-based recommendations within delegated authority.
• Leads workstreams and begins project leadership; impact spans multiple products or markets with material delivery and compliance implications.

Experience Required

• Typically 3–5 years in Regulatory Affairs; relevant scientific or technical degree preferred.
• Ability to represent Regulatory in project teams and lead defined workstreams with increasing independence.
• Practical experience across lifecycle submissions, dossier maintenance, and cross-functional issue resolution.

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 Total Rewards 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 here.

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.

About the Role

This role offers the opportunity to make a meaningful contribution within the Regulatory Affairs organisation, supporting product availability and regulatory performance while further developing your regulatory expertise, business knowledge, and professional capabilities in a dynamic global environment.

Qualifications

Preferred qualifications include:

• Relevant scientific or technical degree.
• Experience in Regulatory Affairs.

Skills

• Strong understanding of regulatory requirements and processes.
• Excellent problem-solving and decision-making skills.
• Effective communication and stakeholder management skills.
• Ability to work independently and collaboratively.
• Proficiency in Microsoft Office and other relevant software.

Benefits

We offer a comprehensive benefits package including:

• Competitive compensation.
• Flexible hybrid working approach.
• Supportive and inclusive culture.
• Career development opportunities.
• Employee assistance programs.
• Health and wellness programs.

Pay

The salary range for this role is $70,000 - $100,000 annually, depending on experience and qualifications.

Schedule

The role is currently available on a full-time basis, with the option to work remotely two days per week.