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Senior Global Regulatory Affairs Leader (a)

Basel-Country Permanent View Job Description
Our client is seeking a senior Regulatory Affairs professional to drive EU and global regulatory strategies across complex development and lifecycle programmes. This role combines strategic leadership, health authority interaction, submission oversight, and cross-functional project leadership in an international environment.

Added 12/10/2026

  • Lead EU and global regulatory strategy for innovative programmes
  • High-impact role with broad cross-functional visibility

About Our Client

Our client is a leading international pharmaceutical organisation with a strong global presence and a commitment to improving patient access to healthcare solutions. Due to ongoing business needs and portfolio growth, they are looking for an experienced regulatory leader who can join the team with a quick start. Hybrid work model.

Job Description

  • Define and execute EU and global regulatory strategies aligned with development objectives
  • Act as the primary regulatory contact for European health authorities and coordinate regulatory interactions
  • Lead regulatory agency meetings, scientific advice procedures, and preparation of briefing documentation
  • Oversee preparation and submission of regulatory dossiers throughout the product lifecycle
  • Drive global submission planning, execution, and regulatory milestone delivery
  • Ensure compliance of product information and labelling activities across markets
  • Represent Regulatory Affairs within cross-functional project teams and governance forums
  • Monitor evolving regulatory requirements and assess business impact
  • Provide regulatory expertise for business development, partnerships, and due diligence activities
  • Lead regulatory sub-teams and support affiliates and external partners on strategic regulatory matters



The Successful Applicant

  • Master's degree in Life Sciences, Pharmacy, Biotechnology, or a related scientific discipline
  • Minimum 8 years of Regulatory Affairs experience within the pharmaceutical or biotechnology industry
  • Strong expertise in EU regulatory procedures and global regulatory frameworks
  • Proven experience interacting with EMA and European health authorities
  • Deep understanding of clinical development, registration pathways, and lifecycle management
  • Demonstrated leadership skills within complex international projects
  • Excellent stakeholder management, communication, and influencing abilities
  • Fluent English, both written and spoken
  • Ability to work effectively in cross-functional and global matrix environments



What's on Offer

  • Strategic regulatory leadership position
  • International and highly visible role
  • Broad exposure to EU and global regulatory activities
  • Hybrid work model (3 days onsite, 2 days HO)



Quote job ref
JN-102026-7123784

Job summary

Job Function
Healthcare & Life Sciences
Specialisation
Regulatory Affairs
Industry
Healthcare / Pharmaceutical
Where
Basel-Country
Contract Type
Permanent
Job Reference
JN-102026-7123784

Michael Page is an equal opportunity employer committed to workforce diversity, both as an employer as well as a recruitment service provider. Each recruitment decision we make for people we hire and people we place into new roles is based solely on the candidates’ knowledge, experience and skills.