Global Head of Regulatory Strategy

2 weeks ago


Cambridge, United Kingdom Mundipharma Full time

Global Head of Regulatory Strategy & Labelling

Location: Cambridge, Hybrid - Open to remote working

Department: Regulatory Affairs

Job type: Full Time

Join us and make a difference when it matters most

At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.

The Team

Global Head of Regulatory Strategy & Labelling will join the Senior Leadership team in the Regulatory Affairs department at Mundipharma being accountable for global regulatory strategic leadership and CCDS and labelling updates. The Global Head will ensure efficient, effective leadership, management and delivery of regulatory strategy and labelling strategy for the full portfolio across the product lifecycle being accountable for the internal RA strategy lead team and for oversight for outsourced RA activity.

Role and Responsibilities

The Global Head of Regulatory Strategy & Labelling will have a clinical strategy focus on regulatory strategy on both marketed products and ongoing clinical development. Main responsibilities for the role will include:
- Accountable for overall Regulatory Strategy for all products including effective deployment of specific regulatory expertise to ensure portfolio regulatory deliverables are met, alignment of the strategy with RA CMC and the market clusters. Accountable for the regulatory stewardship of assets in clinical development and for labelling strategy across the product lifecycle and portfolios.- Accountable for the successful execution of the regulatory strategy with nimble and proactive leadership of regulatory strategy revisions based on availability of new data or changes in company/commercial position. Responsible for generating global regulatory strategy plans for all products in the portfolio- Proactive engagement with stakeholders and senior leaders in the development of regulatory strategies and delivery of regulatory expertise and results in line with Commercial goals. Engagement with external experts and consultants as needed to support regulatory strategic decision making.- Ensure that regulatory and Regulatory strategies fully recognise risk, provide mitigations and ensure that these are communicated and acknowledged within the organisation for appropriate decision-making- Accountable for optimal engagement with Regulatory Authorities in developing Mundipharma’s assets and ensuring Regulator feedback and requirements are understood and adequately reflected in product strategic and tactical plans- Accountable for regulatory contribution and oversight of promotional materials. Representing Regulatory as a core member of the Signal Evaluation and Labelling Group. Accountable for regulatory intelligence

What you’ll bring- Proven experience in Pharma Regulatory Affairs strategy and experience in managing labelling activities- A track record of developing and executing innovative regulatory strategies and leading successful interactions with key Health Authorities such as EMA, FDA, BfArM, MHRA, TGA, PMDA etc- An excellent regulatory strategist with strong commercial instincts and demonstrated ability in delivering superior regulatory outcomes across a diverse product portfolio.- Strong understanding and expertise in Clinical Strategy- Demonstrated knowledge in labelling strategy and management of product labels across the product lifecycle.- Excellent collaborator with strong customer and stakeholder focus. Able to build relationships and inspire confidence and respect at all levels, Including with senior leaders within the organisation.

What we offer in return- Flexible benefits package- Opportunities for learning & development through our varied programme- Collaborative, inclusive work environment

Diversity and inclusion

Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. We believe this isn’t just the right thing, but also the smart thing to do. We are on a journey and will seek to move forward together through education and awareness to build a culture that welcomes and celebrates diversity and uniqueness. We will create a workplace environment where everyone can, every day, bring their authentic selves and is treated with dignity and respect.

About Mundipharma

Mundipharma is a global healthcare company focussing on customers across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.

Join our talent pool

If you’re not sure this role is right for you but you’re keen to hear about future opportunities at Mundipharma,

join our talent community

and be the first to hear about new roles.

Additional Job Description:
Primary Location:
GB Cambridge

Job Posting Date:
2025-09-05

Job Type:
Permanent



  • Cambridge, United Kingdom AstraZeneca Full time

    A leading pharmaceutical company seeks a Senior Regulatory Affairs Director to drive the global regulatory strategy of their innovative products. This role demands a strategic leader with substantial experience in regulatory affairs, aiming to ensure rapid approval and compliance across global markets. The ideal candidate will possess a deep understanding of...


  • Cambridge, United Kingdom AstraZeneca Full time £125 - £150

    A leading pharmaceutical company seeks a Senior Regulatory Affairs Director to drive the global regulatory strategy of their innovative products.Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.This role demands a strategic leader with substantial experience in regulatory affairs, aiming to...


  • Cambridge, United Kingdom AstraZeneca Full time £125 - £150

    A leading pharmaceutical company seeks a Senior Regulatory Affairs Director to drive the global regulatory strategy of their innovative products.A variety of soft skills and experience may be required for the following role Please ensure you check the overview below carefully.This role demands a strategic leader with substantial experience in regulatory...


  • Cambridge, United Kingdom VRS Regulatory Full time

    We are looking for an experienced agrochemical regulatory ecotoxicologist to work as a technical specialist in a multi-disciplinary registrations team. The role will require a high level of understanding of regulatory requirements and risk assessment strategy for products and active substances in accordance with EU requirements. The role will involve...


  • Cambridge, United Kingdom AstraZeneca Full time

    The Head of (Executive Director) International CMC Regulatory Affairsreports to the VP International Regulatory Affairs and is accountable for leading a team of Regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy delivery and execution of International CMC Regulatory strategy and leadership...


  • Cambridge, United Kingdom PE Global Full time

    **PE Global is currently recruiting for a Regulatory Affairs Consultant for a leading multi-national pharmaceutical client based in Cambridge.** **The Regulatory Affairs Consultant will be responsible for the local coordination and execution of regulatory submissions in compliance with corporate standards and national regulatory requirements, and of...


  • Cambridge, United Kingdom Mundipharma International Full time £150 - £200

    Apply (by clicking the relevant button) after checking through all the related job information below.**Regulatory Affairs Head of CMC****Location:** Cambridge**Department:** Regulatory Affairs**Job type**: PermanentJoin us and make a difference when it matters most!At Mundipharma, we are proud of the work we do to bring innovative treatments to patients.We...


  • Cambridge, United Kingdom Mundipharma International Full time £150 - £200

    Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.**Regulatory Affairs Head of CMC****Location:** Cambridge**Department:** Regulatory Affairs**Job type**: PermanentJoin us and make a difference when it matters most!At Mundipharma, we are proud of the work we do to bring innovative treatments...


  • Cambridge, United Kingdom Quanta part of QCS Staffing Full time

    Senior Manager Regulatory Affairs - Pharmaceuticals - Cambridge Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Senior Manager Regulatory Affairs. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to join...


  • Cambridge, Cambridgeshire, United Kingdom Mundipharma Full time

    Regulatory Affairs Head of CMC Location: CambridgeDepartment: Regulatory AffairsJob type: PermanentJoin us and make a difference when it matters mostAt Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our...