Director, Labelling Strategy and Development

GSK

1d•€111,750 - €186,250•Hybrid

About The Position

As Director, Global Regulatory Labelling Strategy and Governance, you will lead the strategy and execution of product labelling for assigned assets within GSK’s vaccines and infectious diseases portfolio. You will oversee the development of clear, compliant, and patient-focused labelling across the product lifecycle—from early development through lifecycle management. In this role, you will line manage a small team of labelling professionals and collaborate closely with cross-functional partners across regulatory, clinical, safety, medical, and commercial functions. You will play a critical role in translating complex scientific data into effective product information and influencing labelling strategy at a global level. This position offers high visibility, strategic impact, and the opportunity to help shape labelling practices that ultimately support patients worldwide.

Requirements

Bachelor’s degree in life sciences, pharmacy, medicine, or a related discipline.
5+ years of labelling or regulatory experience within the pharmaceutical or biotechnology industry.
Demonstrated experience leading global and regional labelling strategy (US PI, EU SmPC) for pharmaceutical products.

Nice To Haves

Advanced degree (MS, PharmD, MD, or PhD) in a relevant scientific discipline.
Experience line managing and developing teams within labelling or regulatory functions.
Direct experience engaging with health authorities and supporting regulatory submissions.
Experience in vaccines, infectious diseases, or related therapeutic areas.
Experience working in cross-functional, matrixed organizations.
Proven ability to interpret clinical and safety data and translate it into regulatory-compliant labelling.
Willingness and ability to work in a hybrid environment with regular onsite collaboration (2–3 days per week).
Demonstrated ability to develop clear, patient-friendly, plain-language labelling content.
Strong written and verbal communication skills, with experience presenting to senior stakeholders.

Responsibilities

Lead global labelling strategy and execution for assigned assets across development and lifecycle stages.
Line manage, coach, and develop a small team of global labelling professionals, building capability and engagement.
Translate clinical and safety data into clear, compliant, and patient-focused labelling content.
Partner with cross-functional teams (regulatory, clinical, safety, medical, and commercial) to align on labelling strategy and deliverables.
Represent the portfolio in labelling governance bodies and ensure alignment with global regulatory requirements and internal standards.
Provide strategic labelling guidance to project teams and senior stakeholders, including implications for development plans and regulatory submissions.
Engage with health authorities, external stakeholders, and professional organizations to support regulatory interactions and contribute to the evolution of labelling practices.