Head of Regulatory Life Cycle Management

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...

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...

Novo Nordisk A/S is seeking a skilled Regulatory Data Manager to join our team. The successful candidate will be responsible for defining and maintaining data standards, policies, and procedures to ensure data quality, security, and compliance with regulatory requirements.As a Regulatory Data Manager, you will be responsible for collaborating with...

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...

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...

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...

Category: Reg Affairs & Safety PharmacovigilanceLocation: Søborg, Capital Region of Denmark, DKAre you able to cut through complexity and drive regulatory strategies for high impact projects? Would you like to work together with experts across multiple functions in a global environment? Do you want to be part of an exciting area where engaged people are...

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 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...

At Novo Nordisk A/S, we are seeking a highly skilled Regulatory Affairs Professional to join our team. This role will play a key connection between scientists and Health Authority regulators, ensuring fast and successful regulatory submissions and approvals in all global markets.About the RoleThis is an exciting opportunity for a talented individual to join...

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 UsWe are a global pharmaceutical company committed to creating innovative solutions for better lives.Our Regulatory Affairs team plays a crucial role in ensuring the safe and effective use of our products.Job DescriptionKey Responsibilities:Develop and implement process strategies to drive excellence in regulatory affairsManage cross-functional...

At Novo Nordisk A/S, we are expanding our product and project pipeline in a fast-paced, dynamic environment.We are 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 in the RA CMC Biotech & Rare Disease area.The ideal...

Are you passionate about working with data? Do you want to set directions and deliver results? Do you have the ability to handle complex tasks? If yes, we are seeking an experienced and highly motivated Regulatory Data Partner to join our team, who will be responsible for implementing and supporting our data in the Regulatory organisation, and support...

Are you passionate about working with data? Do you want to set directions and deliver results? Do you have the ability to handle complex tasks? If yes, we are seeking an experienced and highly motivated Regulatory Data Partner to join our team, who will be responsible for implementing and supporting our data in the Regulatory organisation, and support...

We are looking for a Head of Quality Team to join our Digital Health & Staffs Quality department at Novo Nordisk A/S. This is a fantastic opportunity for a motivated and results-driven individual to take on a leadership role and drive business growth.The successful candidate will have a strong understanding of quality management systems and regulatory...

Job DescriptionAs a Regulatory Affairs Professional, you will play a key role in ensuring fast and successful regulatory submissions and approvals in all global markets. You will join an experienced team working with oral products, focusing on RA CMC life-cycle management activities.Your main responsibilities will include:Planning, coordinating, and...

Novo Nordisk is driving change in the industry by embracing experimentation and striving for excellence without fixating on perfection. We're a dynamic company in a fast-paced environment, working together to move the needle on patient care.Job DescriptionThis is an opportunity to work on synthetic small molecules, including process design, analytical...

Company OverviewNovo Nordisk A/S is a leading global healthcare company focused on driving innovation and making a meaningful difference in people's lives.Our commitment to excellence drives us to push boundaries and strive for outstanding results.Job SummaryThis role is responsible for driving process excellence and digital transformation in regulatory...