Strategic Regulatory BD Role for Medicinal Products

Select 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...

Select 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...

About the Role">This position offers the chance to work on exciting projects and contribute to Business Development (BD) activities across Novo Nordisk's therapeutic areas, representing Global Regulatory Affairs within the Global Project BD Team.">You will be responsible for leading Regulatory BD activities and establishing a Matrix Team covering all...

Key Responsibilities">This role requires a high level of leadership, utilizing communication prowess across organizational tiers, and fostering valuable professional networks that include external collaborations. The ideal candidate will have a keen analytic mindset, identifying value-critical paths and planning future projects.You will collaborate with the...

About the Department">The Regulatory Affairs Diabetes and Obesity therapeutic area is responsible for creating global regulatory strategies to advance projects from the early stages of development to worldwide submissions and approvals of initial Marketing Authorisation applications.">As a key member of this team, you will collaborate with cross-functional...

Job Overview">We are seeking a highly skilled and experienced Regulatory Affairs professional to join our team as a Regulatory Affairs Strategic Development Director. In this role, you will be responsible for leading the development and implementation of regulatory strategies to support the commercialization of medicinal products.The ideal candidate will...

Job Overview:Novo Nordisk A/S is seeking a skilled and experienced Regulatory Affairs Business Development Director to lead RA BD activities and collaborate with the BD Director and regulatory specialists to evaluate external assets and companies for in-licensing, partnerships, or acquisitions across NN's therapeutic areas.The successful candidate will be...

Job Description">In this role, you will be responsible for evaluating external assets and companies for in-licensing, partnerships, or acquisitions across Novo Nordisk's therapeutic areas. You will also serve as a strategic business partner within global Regulatory Affairs in relation to Novo Nordisk's existing portfolio and lead portfolio-wide...

About UsNovo Nordisk A/S is a world-leading biopharmaceutical company with over 90 years of experience in delivering innovative medicines that improve the lives of people with diabetes and other serious chronic conditions. Our mission is to create value for patients, customers, and shareholders through sustained growth, customer satisfaction, and operational...

About UsWe are committed to securing process excellence and digital innovation to reach more patients faster by simplifying and standardizing ways of working with a focus on end users. Our Regulatory Affairs team manages submission, registration, and labelling to obtain authority approval for all Novo Nordisk products. We work across the value chain from...

Job OverviewWe are looking for a talented Regulatory Affairs Professional to join our team at Novo Nordisk A/S. This is an exciting opportunity to work on innovative solutions to complex CMC manufacturing strategies and regulatory requirements.About the PositionThis position plays a key role in making medicines available to patients around the world by...

We're committed to creating an inclusive culture that celebrates diversity and promotes equality of opportunity for all job applicants. At Novo Nordisk, we recognize that being the best company in the world is no longer good enough; we need to aspire to be the best company for the world.About the RoleAs a CMC Regulatory Specialist, you'll contribute to...

CMC Regulatory Strategy LeadAbout Our CompanyNovo Nordisk A/S is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient...

Job Title: Global Regulatory Lead in CVD/CKD Area - Strategic ExpertWe are seeking a highly skilled and experienced professional to join our team as a Global Regulatory Lead. As a key member of our cross-functional project teams, you will be responsible for driving regulatory strategies and executing various regulatory tasks.The successful candidate will...

Company Overview">At Novo Nordisk A/S, we strive to be a leader in diabetes care and innovative biopharmaceuticals. Our company has been committed to improving the lives of people with diabetes for more than 90 years.We are dedicated to developing innovative medicines that make a meaningful difference to patients' lives, from early discovery to late-stage...

At Novo Nordisk, we are expanding our product and project pipeline and seeking an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join the Synthetics & Cell Technologies Department. This role provides strategic, tactical, and operational regulatory input to projects.The...

About the Role\This exciting opportunity is part of Novo Nordisk's Global Regulatory Affairs team. As a Regulatory Specialist, you will play a key role in shaping the company's regulatory strategies and ensuring compliance with regulatory requirements.\Key Responsibilities:\\Develop and implement effective regulatory strategies to support the development and...

Select how often (in days) to receive an alert: Create Alert (Senior) Regulatory Affairs Professional, RA Obesity - Maternity cover Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you have a talent for navigating complex regulatory landscapes and driving strategic initiatives? Are you eager to contribute...

Select how often (in days) to receive an alert: Create AlertCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKDo you want to be part of a growing organization, contributing to the success of Novo Nordisk's expanding product portfolio? Are you passionate about regulatory guidelines and committed to ensuring...

About Our TeamWe are a diverse and inclusive team of professionals dedicated to delivering high-quality products and services. Our team is passionate about innovation and quality, and we are committed to creating a culture of excellence.We are seeking a Senior Quality Assurance Specialist to join our CMC API QA team. In this role, you will be responsible for...