Join VCLS in Copenhagen as Associate Director – Health-tech LCM
Shape the future of health innovation in the Nordics and beyond
Are you an experienced Regulatory professional with ambitions to make a real difference — both locally and globally?
At VCLS, we’re looking for an Associate Director – Health-tech LCM to strengthen our Nordic presence and advise some of the world’s most innovative biotech and pharma companies.
This is an opportunity for someone who thrives at the intersection of science, strategy, and business — and who wants to help drive the development of the next generation of health-tech solutions.
Why join VCLS?
At VCLS, we’re more than consultants — we are trusted advisors, helping life science companies bring innovation safely to patients.
As Associate Director, Consulting for Health-tech Products LCM, you’ll play a key role in:
- developing and implementing regulatory strategies for marketed products,
- collaborating with both Nordic and international clients,
- and leading a team of skilled consultants in an environment defined by expertise, flexibility, and impact.
You’ll join a global network with a strong local base in Copenhagen — and have the opportunity to influence both our Danish business and your own professional growth.
What you’ll do
Strategic advisory and LCM leadership
- Act as a trusted advisor to our Nordic clients on regulatory requirements and strategies.
- Deliver evidence-based recommendations that bring value to clients and authorities.
- Combine compliance and innovation — and stay ahead of both local and global trends.
Client development and partnerships
- Build long-term relationships based on trust, insight, and quality.
- Translate complex regulatory challenges into clear, business-oriented solutions.
- Identify and seize new opportunities for collaboration and growth in the Nordics.
Project leadership and team development
- Lead cross-functional projects with focus on quality, delivery, and collaboration.
- Take ownership of project scope, timelines, and budget — and deliver with precision.
- Mentor and support junior colleagues, contributing to a learning and growth-oriented culture.
Why VCLS?
At VCLS, you’ll find:
- A role with real responsibility and influence — in both projects and business development.
- An international environment where scientific depth meets strategic thinking.
- A culture built on trust, flexibility, and collaboration.
- Opportunities to work with some of the most exciting and complex products in the life science industry.
Ready to take the next step in your career — and help shape the future of health innovation?
Apply now and join the Nordic team at VCLS in Copenhagen.
Requirements
- At least 8 +years’ experience in Regulatory Affairs — preferably with consulting experience.
- Strong knowledge of Nordic and global regulatory frameworks (EMA, FDA, national authorities).
- Strategic and analytical mindset, paired with a practical, solution-driven approach.
- An established network within the life science industry and confidence engaging senior stakeholders.
- Experience in project management, client development, and team leadership.
- Fluency in Danish and English, written and spoken.
Top Skills
What We Do
From discovery to product launch and lifecycle management
At VCLS (Voisin Consulting Life Sciences), regulatory science guides Biotechnology, Pharmaceutical and Medtech manufacturers throughout product development and commercialization. Starting early in the process, from discovery to the patient, VCLS assists innovators in designing optimized product development plans and regulatory strategies, combining the health ecosystem with commercial success. With a presence in seven locations across three continents and over 200 employees, VCLS serves a broad range of healthtech developers and their investors.
Together, we accompany global stakeholders to expedite HealthTech products from discovery to patient access and beyond by bridging Science to Regulatory and Market Access strategies.
