Associate Director, Life Cycle Management

Shape the future of health technology – and be the strategic driver behind global LCM strategies

As Associate Director, Consulting for Health-tech Products LCM at Voisin Consulting Life Sciences (VCLS), you will play a pivotal role in driving strategic regulatory life-cycle management (LCM) within the biotech and pharmaceutical industries. 

With a direct report to the Group Leader in France, you will combine deep regulatory expertise with high-level strategic consulting, advising both executive leadership and cross-functional teams within the VCLS clients’ organisations. You will serve as a trusted advisor to top-tier life science clients and mid-sized biopharma, shaping and driving regulatory LCM strategies in Nordic countries and worldwide.

Your key responsibilities will include:

  • Acting as a strategic advisor to clients across the entire LCM landscape, defining regulatory and business pathways for market optimisation
  • Developing and leading overarching regulatory roadmaps for complex, global portfolios
  • Deliver complex, multi-stakeholder projects with precision, adaptability, and accountability
  • Managing stakeholders across R&D, clinical teams, marketing, and compliance – both internally and externally
  • Representing clients before regulatory authorities and senior-level stakeholders, ensuring alignment with business objectives
  • Monitoring global regulatory changes and translating them into proactive strategies
  • Contributing to business development activities, including proposal preparation, thought leadership, and the development of new service offerings

You are the right fit if you:

  • Have at least 10 years of experience in regulatory affairs, including solid Life Cycle Management expertise in health-tech products (pharma, biotech, medical devices, or combination products) – preferably in a consulting environment. with an Industry network in the Nordics
  • Have solid experience working as a consultant in strategic advisory roles, leading and influencing clients and projects, interacting with senior stakeholders
  • Deep understanding of local Nordic Regulatory Frameworks and proven experience in interacting with regulatory authorities in both the EU and the US
  • Thrive in a role where you can work both analytically and visionary, turning complex requirements into clear, actionable plans
  • Hold a relevant life sciences degree (e.g. pharmacist, biologist, engineer, or equivalent)
  • Are an excellent communicator who can build trust and engagement with clients and colleagues at all levels

Voisin Consulting Life Sciences offers you the opportunity to join a global consulting environment where you collaborate with some of the most innovative health-tech companies in the world. Working in a dynamic, international matrix environment, your contributions will directly impact healthcare outcomes, regulatory success, and client satisfaction. VCLS offers a flexible work environment and plenty of opportunities for personal growth across the organisation.

Travelling: A few days a year for events. Working on-site with clients occasionally is part of the job.

Domicile: Copenhagen, Denmark. 

At Unique Human Capital, we are committed to promoting diversity and including all perspectives. Thus, we encourage all qualified candidates to apply for the position. Please enclose your CV in English.

Søg dette job

Gå tilbage til oversigten

Følg os