At a Glance
- Tasks: Lead regulatory strategy for medicines, ensuring compliance and high-quality outcomes.
- Company: Join Perrigo, a top player in consumer self-care, dedicated to making lives better.
- Benefits: Enjoy competitive pay, family support, and flexible hybrid working options.
- Other info: Be part of an inclusive culture that values collaboration and continuous improvement.
- Why this job: Make a real impact on product availability and consumer health while leading a dynamic team.
- Qualifications: Advanced degree in life sciences and significant regulatory affairs leadership experience required.
The predicted salary is between 75000 - 90000 £ per year.
- Director - 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®, Ni Quitin®, 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 a Director – Regulatory Affairs Lifecycle Management Medicines. This is a newly created role within Perrigo Scientific Office.
As the leader of lifecycle management for medicines you will be a senior leader driving the delivery of Perrigo’s global regulatory strategy across the full product lifecycle.
You will shape and execute robust regulatory strategies, ensuring the consistent delivery of high-quality regulatory outcomes across a diverse and complex portfolio.
You will hold end-to-end accountability for lifecycle management activities, overseeing the development, submission, and maintenance of regulatory dossiers to meet global requirements and business priorities.
Through strong leadership and decision‑making, you will anticipate risks, define mitigation strategies, and ensure timely, compliant submissions that protect supply continuity, consumer safety and enable market access.
Leading a high‑performing team, you will set clear direction, build capability, and foster a culture of ownership, accountability, and continuous improvement.
You will ensure effective prioritisation and execution across competing demands, aligning regulatory activities with broader organisational objectives.
As a key partner to cross‑functional stakeholders – including Quality, Safety, Supply Chain and R&D – you will provide regulatory leadership on change management and business strategy insights, ensuring alignment between technical, operational, and regulatory requirements.
Your ability to translate complexity into clear, actionable direction will be critical in supporting business performance and portfolio optimisation.
You will also play a central role in strengthening the Regulatory Affairs function and ways of working, driving efficiency, consistency, and scalability across lifecycle processes.
Through your expertise and influence, you will ensure Perrigo continues to meet evolving regulatory expectations while maintaining the highest standards of compliance and quality.
This is a highly visible role within the Regulatory Affairs organisation, offering the opportunity to make a tangible impact on product availability, regulatory performance, and consumer outcomes – while developing and leading a team that delivers excellence at scale.
- Scope of the Role
- Leading a major lifecycle management capability with enterprise or broad regional impact.
- Defining the operating model, governance, performance standards, and transformation roadmap for post-approval and operational delivery.
- Accountable for strategic outcomes, compliance posture, talent, and transformation initiatives across lifecycle‑management interfaces within the regulatory function and PSO organisation.
- Own the enterprise lifecycle management operating model activities within scope and set standards, metrics, and governance for post‑approval, CMC/Business strategy, and operations.
- Ensuring inspection readiness, dossier integrity, right‑first‑time submission operations, vendor or outsourcing strategy, and scalable processes and data governance.
- Influencing enterprise strategy and external environment; operates with enterprise‑scale complexity and accountability through leaders and specialist teams.
- Capability Leadership & Operating Model
- Define and lead the operating model, governance, and performance standards for lifecycle management, within scope.
- Set direction for post‑approval strategy, major change programmes, remediation, portfolio resilience, and enterprise compliance priorities.
- Ensure alignment across lifecycle management, category, cluster, and regulatory operations so regulatory decisions translate into executable, compliant outcomes across markets.
- Own standards for dossier quality, decision logs, implementation governance, inspection readiness, and right‑first‑time delivery.
- Lead major improvement, digital, and data‑driven initiatives that strengthen execution, predictability, and scalability.
- Own major compliance and supply risk posture within scope and ensure appropriate governance, escalation, crisis readiness, and resilience.
- Set metrics, dashboards, and management rhythm for performance and intervene where results, capability, or control require strengthening.
- Manage vendor or outsourcing strategy where relevant to lifecycle management, or operational delivery.
- Lead leaders and specialist teams, setting culture, capability expectations, and succession plans.
- Represent the capability in senior enterprise forums and influence business strategy through clear regulatory insight, risk framing, and operating model leadership.
- Build strong relationships with senior internal stakeholders and with external authorities or industry bodies where relevant to significant lifecycle matters.
Experience Required
- Bachelor’s degree or higher in life sciences, pharmacy, or related discipline; advanced degree preferred.
- Significant experience in progressive regulatory affairs leadership across portfolios, regions, or capabilities.
- Proven leadership in enterprise portfolio delivery, governance ownership, operating model design, and transformation.
- Demonstrated Areas of Expertise
- Enterprise Leadership – sets direction, aligns stakeholders, and delivers outcomes through leaders and teams.
- Strategic Foresight – anticipates regulatory trends and builds proactive plans and policy positions where appropriate.
- Governance & Risk Ownership – establishes enterprise governance, quality standards, and compliance posture and manages major risks and crises.
- Transformation – leads digital and operational transformation and capability building and measures impact and sustainability.
- External Engagement – builds credible relationships with authorities and industry and represents the organisation with integrity.
- Talent & Culture – builds diverse capability, develops succession, and fosters continuous improvement.
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 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.
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StudySmarter Expert Advice🤫
We think this is how you could land Director - Regulatory Affairs Lifecycle Management Medicines
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We think you need these skills to ace Director - Regulatory Affairs Lifecycle Management Medicines
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Perrigouk!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Perrigouk that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Perrigouk!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Perrigouk, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Perrigouk
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Perrigouk that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Perrigouk’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.