CMC Expertise Role

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...

Regulatory Affairs Leader for Biologics and Rare DiseasesAbout Our TeamThe newly established RA CMC BRD Development Projects & LCM is one of three areas in RA CMC Biologics & Rare Diseases, which is a VP area organized in the RA CMC & Device organization with 270 employees.Our VisionAs Director, you will lead and develop leaders and specialists organized in...

Director of Regulatory Affairs for CMC Biologics & Rare DiseasesCategory: Project Management & AgileLocation: Søborg, Capital Region of Denmark, DKAre you an experienced purpose-driven and business-minded second line leader with extensive expertise in drug regulatory affairs? Do you excel in a dynamic environment and want to be part of a rapidly growing...

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 are seeking an experienced purpose-driven and business-minded second line leader with extensive expertise in drug regulatory affairs to join our team as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the roleAs the Director for RA CMC Biologics & Rare Diseases, you will play a pivotal role in shaping the future of RA CMC. We are...

Select how often (in days) to receive an alert: Create AlertCategory: Reg Affairs & Safety PharmacovigilanceLocation: Søborg, Capital Region of Denmark, DKWe are expanding our product and project pipeline in Novo Nordisk and are looking for an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic...

About the RoleWe are looking for a skilled and experienced Regulatory Compliance Expert to join our CMC API QA team.In this role, you will be responsible for ensuring compliance with regulatory requirements, quality standards, and company policies in the manufacturing of APIs.You will also participate in regulatory inspections and audits, and ensure that our...

About the TeamClinical Trials Operations is a department that employs over 40 skilled and motivated colleagues. We work together to assure quality and compliance of the CMC API facilities & equipment and release of raw materials, cell banks, and API for clinical trials. Our team values teamwork, diversity, and humour, and we strive to create an inclusive...

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...

JobbeskrivelsePlaceringBagsværd, DenmarkJobkategoriQualityAnsøg nuDo you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in ensuring the quality and safety of products for clinical trials and thereby secure and support the development pipeline in Novo Nordisk?...

Director of Regulatory Affairs for CMC Biologics & Rare DiseasesAbout the PositionThe RA CMC organization is growing, and we are strengthening our leadership team with a new Director with strong experience and interest in Regulatory Life Cycle Management. As the Director for RA CMC Biologics & Rare Diseases, you will play a pivotal role in shaping the future...

Global Regulatory CMC Leadership RoleAbout Our CultureWe recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures.About the JobWe are seeking a highly...

We are looking for a dynamic and visionary leader to spearhead our team as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the positionThe RA CMC organization is growing, and we are strengthening our leadership team with a new Director with strong experience and interest in Regulatory Life Cycle Management.Be accountable for the...

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...

We are committed to finding the best candidate for this exciting opportunity as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the departmentThe newly established RA CMC BRD Development Projects & LCM is one of three areas in RA CMC Biologics & Rare Diseases, which is a VP area organized in the RA CMC & Device organization with 270...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Professional to join our RA CMC & Device team. As a key member of our organization, you will play a crucial role in ensuring the success of Novo Nordisk's expanding product portfolio.About the RolePlan, coordinate and execute regulatory submissions.Create, plan and coordinate submission...

Select how often (in days) to receive an alert: Create Alert Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do 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...

We are seeking a highly skilled Regulatory Affairs Professional to join our RA CMC & Device organization, handling RA CMC activities for our marketed Oral Products at Novo Nordisk A/S. As a key member of our team, you will play a vital role in ensuring fast and successful regulatory submissions and approvals in all global markets.The ideal candidate will...

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...

JobbeskrivelsePlacering Bagsværd, DenmarkJobkategori Quality Ansøg nu Would you like to play an important role in ensuring the quality and safety of products for clinical trials, where you can use your solid QA and validation experience in a project context? Then we can offer you a unique position with a lot of responsibility and impact in a dynamic and...