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.