Regulatory Affairs Business Development Strategist
5 days ago
At Novo Nordisk, we are committed to creating innovative solutions to improve the lives of patients worldwide.
Company OverviewWe strive to be a leader in our industry by pushing boundaries, embracing new technologies, and fostering a culture of collaboration and innovation.
The Regulatory Affairs Business Development team is responsible for evaluating external assets and companies for in-licensing, partnerships, or acquisitions across Novo Nordisk's therapeutic areas. As a key member of this team, you will collaborate with regulatory specialists to assess potential opportunities and develop strategies for integration into our global portfolio.
You will work closely with cross-functional groups, including deal teams, and provide direction in matrix teams across Regulatory Affairs. Your expertise in medicinal product development, regulatory strategies, and impact assessments will be invaluable in identifying value-critical paths and planning future projects.
We seek a talented individual who shares our passion for driving change and improving patient outcomes. If you have experience leading project teams through key phases of the product lifecycle and can demonstrate strong interpersonal abilities, analytical thinking, and creativity in problem-solving, we encourage you to apply.
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout the Role:We are seeking a highly skilled Regulatory Affairs Business Development Director to join our team at Novo Nordisk A/S. As a member of our Regulatory Affairs Diabetes and Obesity team, you will play a pivotal role in creating global regulatory strategies to advance projects from the early stages of development to worldwide submissions and...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeSelect how often (in days) to receive an alert: Create Alert Regulatory Affairs Business Development Director Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you have experience developing medicinal products and identifying regulatory risks and opportunities? Are you knowledgeable about the drug...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeSelect how often (in days) to receive an alert: Create AlertRegulatory Affairs Business Development DirectorCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKDo you have experience developing medicinal products and identifying regulatory risks and opportunities? Are you knowledgeable about the drug development...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeCompany Overview:Novo Nordisk A/S is a leading healthcare company that focuses on developing innovative treatments for people with diabetes and other serious chronic conditions. Our vision is to make a significant difference in patients' lives by delivering high-quality products and services.We are committed to fostering a culture of innovation,...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeJob Description:We are seeking a highly skilled Regulatory Affairs Business Development Director to join our team at Novo Nordisk A/S.The successful candidate will have a strong background in regulatory affairs and business development, with experience in evaluating external assets and companies for in-licensing, partnerships, or acquisitions. They will also...
-
Regulatory Affairs Strategist
4 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout Novo Nordisk A/SWe are a dynamic company in an even more dynamic industry, always striving to drive change and move the needle on patient care.Our team is responsible for developing and executing global regulatory strategies, advancing projects across multiple indications from early development through worldwide submission and approval.As a Global...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeKey ResponsibilitiesAs a Regulatory Affairs Business Development Director at Novo Nordisk, you will be responsible for:Leading RA BD activities and establishing a Matrix Team covering all relevant regulatory skill areas.Evaluating external assets and companies for in-licensing, partnerships, or acquisitions across Novo Nordisk's therapeutic...
-
CMC Regulatory Affairs Specialist
6 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout the RoleWe are seeking an experienced Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join our team. As a key member of our regulatory affairs department, you will provide strategic, tactical, and operational regulatory input to projects. Your responsibilities will include...
-
Expert in Regulatory Affairs
5 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeSelect how often (in days) to receive an alert: Create AlertExpert in Regulatory Affairs - Primary PackagingCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKAre you ready to take on new challenges in primary packaging development across emerging therapeutic areas and innovative products? Would you like to use...
-
Regulatory Affairs Specialist, RA Obesity
5 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeSelect how often (in days) to receive an alert: Create Alert Regulatory Affairs Specialist, RA Obesity Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Are you passionate about regulatory science and driving innovative regulatory strategies to bring innovative medicines to patients? Do you have strong...
-
Regulatory Affairs Specialist
3 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Reckitt Benckiser Full timeAbout the CompanyWe are Reckitt Benckiser, a global leader in hygiene, health, and nutrition. Our purpose is to protect, heal, and nurture in the pursuit of a cleaner, healthier world.The RoleAs a Regulatory Affairs Associate within our Hygiene division, you will be at the forefront of innovation and compliance efforts. You will work closely with a dynamic...
-
Regulatory Affairs Chemistry Specialist
3 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeJob OverviewWe are seeking an experienced CMC Regulatory Specialist to join our team in Novo Nordisk A/S. As a key member of our regulatory affairs department, you will be responsible for providing strategic, tactical, and operational regulatory input to projects.The ideal candidate will have expertise in synthetic small molecules and experience working with...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout the RoleNovo Nordisk A/S is seeking an experienced Regulatory Affairs Process Excellence Manager to join our RA Process and Digital Strategy area. As a key member of the team, you will play a central role in driving process excellence, innovation, and digital transformation across the regulatory affairs organization at a corporate level and across all...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeSelect how often (in days) to receive an alert: Create Alert Regulatory Affairs Specialist for innovative development within Rare Disease Category: Reg Affairs & Safety Pharmacovigilance Location:Søborg, Capital Region of Denmark, DK Do you want to become part of an exciting environment where engaged people are committed to gain approval of Novo Nordisk's...
-
Regulatory Affairs CMC Professional
4 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout the RoleWe are seeking an experienced Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist to join our Synthetics & Cell Technologies Department in the RA CMC Biotech & Rare Disease area within Novo Nordisk.The successful candidate will provide strategic, tactical, and operational regulatory input to projects, leading activities...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeWe are seeking a highly skilled Professional to join our Regulatory Affairs (RA) Device and Digital Health department at Novo Nordisk A/S. The ideal candidate will have a strong background in regulatory affairs, with expertise in primary packaging development and submission planning.About the Role:This role offers a multi-disciplinary environment with...
-
Regulatory Affairs Associate
4 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Reckitt Benckiser Full timeCity: Soborg We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeJob DescriptionWe are seeking a highly skilled Senior Medical Strategist to join our team in Copenhagen, Denmark. As a key member of our Global Medical Affairs team, you will play a critical role in driving the worldwide strategic direction for Alzheimer's disease treatment.The successful candidate will be responsible for developing and implementing...
-
Global Regulatory Specialist Obesity
4 days ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout This RoleWe are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team within RA Obesity.In this role, you will be responsible for developing and executing late-stage regulatory strategies, collaborating with cross-functional teams, and overseeing regulatory submissions.Key responsibilities may include:Providing...
-
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeJob DescriptionThe role of a Regulatory Affairs Specialist for Innovative Medicine Development in Rare Diseases involves driving regulatory strategies to obtain approvals for novel therapies.As a key member of our Global Regulatory Affairs team, you will work closely with cross-functional project teams to develop and implement regulatory plans that meet the...