Head of Medical Affairs DACH
Nordberg Medical AB, New Bremen, OH, United States
Take part in a journey committed to innovation and improving lives
Nordberg Medical is a Swedish biotech company working at the forefront of biomaterial science to reverse functionality loss. With state‑of‑the‑art biomaterials, we produce and market innovative medical products that target structural imbalances associated with aging.
In 2021, we passed a critical milestone by receiving CE certification for our first product. JULÄINE of Sweden is a biostimulator that activates natural collagen production in the skin. This positions the company well to pursue an ambitious growth strategy in the aesthetic dermatology market.
Backed by leading investors and extensive R&D, we are expanding across multiple therapeutic areas and geographies.
Join an international team of highly talented individuals where your contribution counts. We promote a culture of entrepreneurship, multiculturalism, and flexibility in more than ten countries.
Our Medical Affairs team in Europe is growing and we are looking for our new
Head of Medical Affairs DACH
As our Head of Medical Affairs (HMA) DACH, you will report to our General Manager and lead the medical affairs team in the Germany, Switzerland and Austria. You will be pivotal in establishing strategic and tactical Medical Affairs leadership in your region. You’ll work closely with KOLs, physicians, and healthcare professionals (HCPs) to lead scientific discussions, support trial enrollment and deliver educational programs and training. Serving as the primary medical point of contact, your scientific expertise will be instrumental in enhancing team capabilities and customer interactions.
Your responsibilities will include, but not be limited to:
Key Responsibilities
Reviewing scientific literature to inform company strategy, consolidating actionable medical insights.
Developing regional medical affairs goals, translating them into tactics for optimal scientific exchange.
Managing Key Opinion Leader (KOL) relationships and supporting faculty development activities.
Supporting clinical research (ISS and SIS) by identifying investigators, managing protocols, and reviewing study data. Collaborating with regulatory affairs for submissions and product approvals.
Maintain knowledge of regulatory guidelines and assist in resolving regulatory issues.
Ensuring compliance with local regulations and review promotional materials.
This is a highly collaborative role, where you will be a part of a cross‑functional local team in the DACH region, as well as the global Medical Affairs team. As an early member of the Nordberg Medical team, you’ll have a unique opportunity to contribute to our journey as a global leader in regenerative solutions. You will be required to travel to conferences and attend group meetings on a regular basis.
What you bring to this role
5‑7 Years of successful experience in medical affairs, scientific communications, and / or clinical research ideally within aesthetics, we could consider a medical device of pharma industry background.
Advanced degree in relevant scientific field (MD, PhD, PharmD, etc.).
Strong understanding of combination product (drug and medical device) development and regulatory processes.
Proficiency in German and English with excellent communication skills.
Personality
You approach responsibilities with enthusiasm, and you consistently take the initiative to excel in your work.
You have an adaptive, can‑do attitude, demonstrating both persistence and flexibility when facing challenges.
You thrive in collaborative settings, working seamlessly within cross‑functional teams to drive successful outcomes.
Why should you join our team?
We are a global, inclusive team where innovation and creativity are actively encouraged, empowering you to make a meaningful impact.
An opportunity to develop your career in a dynamic and collaborative environment.
Join us to embark on a journey committed to delivering innovation and improving lives.
#J-18808-Ljbffr
Nordberg Medical is a Swedish biotech company working at the forefront of biomaterial science to reverse functionality loss. With state‑of‑the‑art biomaterials, we produce and market innovative medical products that target structural imbalances associated with aging.
In 2021, we passed a critical milestone by receiving CE certification for our first product. JULÄINE of Sweden is a biostimulator that activates natural collagen production in the skin. This positions the company well to pursue an ambitious growth strategy in the aesthetic dermatology market.
Backed by leading investors and extensive R&D, we are expanding across multiple therapeutic areas and geographies.
Join an international team of highly talented individuals where your contribution counts. We promote a culture of entrepreneurship, multiculturalism, and flexibility in more than ten countries.
Our Medical Affairs team in Europe is growing and we are looking for our new
Head of Medical Affairs DACH
As our Head of Medical Affairs (HMA) DACH, you will report to our General Manager and lead the medical affairs team in the Germany, Switzerland and Austria. You will be pivotal in establishing strategic and tactical Medical Affairs leadership in your region. You’ll work closely with KOLs, physicians, and healthcare professionals (HCPs) to lead scientific discussions, support trial enrollment and deliver educational programs and training. Serving as the primary medical point of contact, your scientific expertise will be instrumental in enhancing team capabilities and customer interactions.
Your responsibilities will include, but not be limited to:
Key Responsibilities
Reviewing scientific literature to inform company strategy, consolidating actionable medical insights.
Developing regional medical affairs goals, translating them into tactics for optimal scientific exchange.
Managing Key Opinion Leader (KOL) relationships and supporting faculty development activities.
Supporting clinical research (ISS and SIS) by identifying investigators, managing protocols, and reviewing study data. Collaborating with regulatory affairs for submissions and product approvals.
Maintain knowledge of regulatory guidelines and assist in resolving regulatory issues.
Ensuring compliance with local regulations and review promotional materials.
This is a highly collaborative role, where you will be a part of a cross‑functional local team in the DACH region, as well as the global Medical Affairs team. As an early member of the Nordberg Medical team, you’ll have a unique opportunity to contribute to our journey as a global leader in regenerative solutions. You will be required to travel to conferences and attend group meetings on a regular basis.
What you bring to this role
5‑7 Years of successful experience in medical affairs, scientific communications, and / or clinical research ideally within aesthetics, we could consider a medical device of pharma industry background.
Advanced degree in relevant scientific field (MD, PhD, PharmD, etc.).
Strong understanding of combination product (drug and medical device) development and regulatory processes.
Proficiency in German and English with excellent communication skills.
Personality
You approach responsibilities with enthusiasm, and you consistently take the initiative to excel in your work.
You have an adaptive, can‑do attitude, demonstrating both persistence and flexibility when facing challenges.
You thrive in collaborative settings, working seamlessly within cross‑functional teams to drive successful outcomes.
Why should you join our team?
We are a global, inclusive team where innovation and creativity are actively encouraged, empowering you to make a meaningful impact.
An opportunity to develop your career in a dynamic and collaborative environment.
Join us to embark on a journey committed to delivering innovation and improving lives.
#J-18808-Ljbffr