Regulatory affairs manager Work, Jobs in Charlwood, Wsx (with Salaries)

Senior Manager Regulatory Affairs Lifecycle Management Medical Devices
Perrigo —London
- Hybrid work
- Bachelor's degree
- In-person
- Leadership
Senior Regulatory Affairs Manager (UK/Ireland)
Perrigo —London
- Hybrid work
- In-person
- Leadership
1d
Manager - Regulatory Affairs Lifecycle Management - Medicines
Perrigo —London
- Hybrid work
- Marketing
- In-person
- Leadership
1d
Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed
PrimeVigilance —Guildford
- Full-time
- Remote
- Nursing
- English
- Microsoft Office
Quick apply
Senior Manager/Associate Director, Government and Regulatory Affairs
Access Partnership —London
- Hybrid work
Quick apply
Senior Manager – ESG and Sustainability Regulatory Legal
Pwc UK —London
- Full-time
- Hybrid work
- Analysis skills
- Presentation skills
Regulatory Affairs Manager
pladis —Chiswick Park Station
- Full-time
ODG Digital Engagement Manager
Hill's Pet Nutrition —Surrey
- £53,100 - £59,000 a year
- Doctoral degree
- Sales
- Marketing
ODG Digital Engagement Manager (175001)
Colgate-Palmolive —Surrey
- £53,100 - £59,000 a year
- Doctoral degree
- Sales
- Marketing
Professional Veterinary Affairs Manager UK & Ireland (175066)
Colgate-Palmolive —Surrey
- £70,650 - £78,500 a year
- Doctoral degree
- Travel
- Up to 25% travel
4d
Associate Director - Regulatory Affairs Operations
Perrigo —London
- Hybrid work
- In-person
- Leadership
Regulatory Quality Assurance Manager
Alliance Medical Ltd —Guildford
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Director, Product and Clinical Training (Hybrid)
Insulet Corporation —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Manager, Quality Assurance - GxP
PTC Therapeutics International Limited —Guildford
- Up to 50% travel
- Microsoft Office
- Bachelor's degree
Quick apply
14d
Independent Maternity Review Programme Support
University Hospitals Sussex NHS Foundation Trust —Worthing
- £57,528 - £64,750 a year
- Full-time
- Leadership
- Annual leave
1d
PV Officer, Team Lead (Japanese Fluency required )
PrimeVigilance —Guildford
- Full-time
- Remote
- Nursing
- English
- Communication skills
Quick apply
Deputy Director for Clean Water and Public Health
Department for Environment, Food and Rural Affairs —London
- £86,000 a year
- Full-time
- Presentation skills
- Travel
- Leadership
8d
Account Manager (Public Affairs)
Hanbury Strategy —London
- Hybrid work
- Project management
- Mentoring
- Leadership
- Health & wellbeing programme
- Annual leave
Commercial Solutions Manager – Drug Delivery Device SME - Remote
Thermo Fisher Scientific —Horsham
- Full-time
- Remote
- Engineering
- Analysis skills
- Project management
14d
Head of Public Policy (UK & Ireland)
Voi Technology —London
- Hybrid work
- English
- Bachelor's degree
- AI
Quick apply

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regulatory affairs manager jobs near charlwood, wsx

Senior Manager Regulatory Affairs Lifecycle Management Medical Devices

Perrigo -
London

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Job details

Qualifications

Change management
Bachelor's degree
Leadership

Full 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®, 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 Senior Manager Regulatory Affairs Lifecycle Management Medical Devices. This is a newly created role within Perrigo's Scientific Office.

As Medical Devices Lead for LCM you will play a key role in delivering Perrigo’s regulatory strategy across the product lifecycle. You will support the development and execution of regulatory strategies, ensuring the consistent delivery of high-quality regulatory outcomes across a diverse and complex portfolio.

You will be responsible for managing lifecycle management activities, overseeing the preparation, submission, and maintenance of regulatory dossiers in line with global requirements and business priorities. You will proactively identify risks, support mitigation planning, and ensure timely, compliant submissions that help maintain supply continuity, consumer safety, and market access.

Leading a team of multi-regional regulatory professionals, you will provide clear direction, support capability development, and foster a culture of accountability and continuous improvement. You will manage priorities across multiple activities, ensuring effective execution and alignment with departmental and organisational goals.

Working closely with cross-functional stakeholders—including Quality, Safety, Supply Chain, and R&D—you will contribute regulatory expertise to change management and business initiatives. You will help translate regulatory requirements into practical, actionable plans that support product maintenance, compliance, and portfolio optimisation.

You will also contribute to the continuous improvement of Regulatory Affairs processes and ways of working, helping to drive efficiency, consistency, and scalability across lifecycle activities. Through your role, you will support Perrigo’s ability to meet evolving regulatory requirements while maintaining high standards of compliance and quality.

This role offers the opportunity to make a meaningful impact within the Regulatory Affairs organisation—supporting product availability and regulatory performance while developing your leadership and technical expertise in a dynamic, global environment.

Scope of the Role

Own regulatory delivery for a defined portfolio or programme across Lifecycle Management and Regulatory Operations interfaces.
Ensures right-first-time submissions, compliant implementation, and robust integration of lifecycle management and operational execution.
Acts as senior advisor and escalation point for regulatory risks, leading a team or matrix workstreams while shaping strategy for higher-complexity lifecycle topics.
Independently assesses and manages complex post-approval changes, renewals, label updates, and implementation controls across the assigned portfolio or programme.
Leads preparation or review of change documentation and response packages under governance and ensures submission publishing readiness, document management, and data integrity.
Owns end-to-end delivery within governance for multi-product portfolio scope with measurable lifecycle and operational outcomes.

Lifecycle & Operational Delivery

Manage post-approval changes, variations, renewals, labels, and implementation controls across the portfolio or programme.
Provide regulatory leadership for relevant changes and responses under governance, ensuring dossier integrity and alignment with lifecycle commitments.
Ensure submission publishing readiness, document control, and system or data integrity in partnership with Regulatory Operations.
Use dashboards, trackers, and metrics to manage workload, cycle times, right-first-time quality, and implementation performance.

Strategy, Governance & Risk

Own regulatory delivery plans, priorities, and risk escalation within scope; approve submission readiness and escalate novel or high-risk issues and major supply or portfolio risks.
Drive process simplification, digital enablement, and continuous improvement across lifecycle and operational delivery.
Ensure disciplined handovers between Category, Cluster, and LCM/Ops and maintain One Regulatory Voice and implementation tracking.

Leadership & Partnership

Lead cross-functional workstreams and develop capability through coaching and matrix leadership.
Partner with Quality, Safety, R&D, Supply Chain, Manufacturing, Artwork, IT/Data, vendors, and Cluster/Category RA to ensure timely, compliant implementation.

Experience Required

Bachelor’s degree or higher in Life Sciences, Pharmacy, or related discipline.
Significant relevant experience in Regulatory Affairs with proven submission and lifecycle delivery; people leadership experience preferred.
Strong regulatory writing, stakeholder management, and operational delivery leadership.

Demonstrated areas of expertise:

Regulatory Expertise & Judgement: Applies sound regulatory and scientific knowledge across classifications and geographies and interprets requirements pragmatically.
Execution Excellence: Plans and delivers end-to-end activities to quality and timelines and drives right-first-time.
Strategic Thinking: Evaluates options and documents rationale and anticipates downstream lifecycle and operational impacts.
Leadership & Collaboration: Leads teams and influences in a matrix, coaches others, and builds capability.
Communication & Influence: Communicates risks and recommendations clearly to senior stakeholders and external partners.
Risk & Compliance Mindset: Proactively identifies and mitigates risks, supports CAPA, and protects continuity of supply.
Continuous Improvement: Improves processes, tools, and ways of working and uses metrics to drive performance.

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. 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

Apply Now

Refine Your Search

regulatory affairs manager jobs in charlwood, wsx

Senior Manager Regulatory Affairs Lifecycle Management Medical Devices

Senior Regulatory Affairs Manager (UK/Ireland)

Manager - Regulatory Affairs Lifecycle Management - Medicines

Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed

Senior Manager/Associate Director, Government and Regulatory Affairs

Senior Manager – ESG and Sustainability Regulatory Legal