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...importance to Novo Nordisk’s growth on a global level.
Apply now for a life-changing career!
The position
As a Regulatory Affairs Professional, you will have the opportunity to work within late-stage development, preparing for upcoming MAA/NDA/BLA submissions...
...focused products? Are you passionate about regulatory science and executing on regulatory... ...The Position
As a Senior Regulatory Affairs Professional, you will collaborate closely... ...various departments, including project management, medical and non-medical specialists, statisticians...
...Are you able to cut through complexity and drive regulatory strategies for high-impact projects? Would you like to work together with... ...functions in a global environment?
Then join Global Regulatory Affairs in Novo Nordisk and be our new Senior Regulatory Professional...
...relevant area? Do you possess a natural interest and flair for regulatory guidelines? Do you enjoy being part of a team where you... ...the people we are looking for.
Novo Nordisk Regulatory Affairs CMC & Device (RA CMC & Device) is on a fortunate journey with...
...the new Data Science Policy Specialist we are looking for in Regulatory Affairs.
We are seeking an enthusiastic specialist to be at... ...support Novo Nordisk’s product development and life-cycle management strategies.
We are a senior team that works closely with...
...timer).
Har du interesse for og meget gerne erfaring med Regulatory Affairs – og helt optimalt med Marketing Compliance - og vil du gerne... ...i København.
Som Regulatory and Marketing Compliance Manager arbejder du tæt sammen med kunder og samarbejdspartnere. Du...
...Category: Regulatory Affairs
Country/Region: DK
Location: Odense, DK, 5260 Søborg, DK, 2860... ...do you have experience in lifecycle management? Then you might be the right match to... ...questions, please contact Department Manager RA LCM CMC Own Sites, Majbritt Eichmeier...
...Are you experienced within device regulatory affairs and are you passionate about finding new pathways for approval of combination products... ...stakeholders in the projects. In addition, an ability to think and manage strategically with attention to detail is needed, as is a...
...medical device industry are increasing and we are a Global Group Regulatory Affairs team of approx. 10 persons who facilitate and actively... ...This position belongs to a HQ function and it is important to manage both HQ and global stakeholders, so they feel confident in the...
...be the individual we are seeking in CTA Management.
Apply now and carve your place in... ....
The position
As an Associate Regulatory Professional for CTA Management at Novo... ...relevant experience working within Regulatory Affairs or Clinical Development/Clinical...
...Novo Nordisk products approved across the globe. In Global Regulatory Affairs, o ur people have a unique combination of scientific insight... ...we support Novo Nordisk’s product development and life cycle management strategies, promoting overall regulatory excellence both...
...Are you passionate about shaping future regulatory frameworks and policies? Do you thrive in... ...for you to join our Global Regulatory Affairs Policy & Intelligence department at Novo... ...Regulatory Policy, you will establish and manage a new team within the Global Regulatory...
...and MICs).
The Technical Specialist (Regulatory, Nutrition) will spearhead regulatory support... ...with strong knowledge of regulatory affairs for nutritional commodities.... ...impact (4) Innovates and embraces change (5) Manages ambiguity and complexity (6) Thinks and...
...about technical writing (incl. IP) and/or regulatory submission process and the subsequent Q&... ...in collaboration with Regulatory Affairs.
You will create documentation for our... ...implementation, optimization, and life cycle management. We offer a very interesting and...
...tasks with challenging timelines? Do you have experience in regulatory affairs or clinical trials? We are looking for a motivated EU Submission... ...across the organization and all countries in Europe
Managing initial clinical trial application submissions in the EU according...
...for a Senior Software Engineer with a focus on the finance and regulatory domains to join our Tech department in Copenhagen or Aarhus.... .... solution considerations, day-to-day processes, requirements management, and stakeholder management.
We welcome all to apply to this...
We are seeking a Data Manager Analytics, with excellent strategic, analytical, technical, stakeholder management, communication and presentation skills, who is eager to share in the successes of a small, dedicated, growth-driven team.
As part of our evolving Data & Insights...
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København
Indrykket for 1 dage siden
...Sr. Regulatory Publisher
(Global Regulatory Publishing, Regulatory Business Operations)
Lundbeck’s passion links to our purpose of... ...We are looking for a Sr. Regulatory Publisher to compile and manage our Regulatory Submissions within Global Regulatory Publishing...
Are you ready your project management experience in an exciting organization... ...As Analytical Project Manager you will play a key role in... ...coordination of analytical validations, regulatory documents, submissions to and... ...Assurance, Regulatory Affairs, and representatives from...
...Are you an experienced Technical Project Manager with a background in medical device development? Are you ready to take on a... ...management, mechanical engineering, , systems engineering, regulatory affairs, and medical & science. You will play an important role in liaising...
