Resultat af søgning: 3.232 ledige stillinger
...Do you have experience from either RA, CMC, QA, and/or QC – or any other relevant area... ...possess a natural interest and flair for regulatory guidelines? Do you enjoy being part of a... ...looking for.
Novo Nordisk Regulatory Affairs CMC & Device (RA CMC & Device) is on a...
...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...
...Apply now for a life-changing career!
The position
As a Regulatory Affairs Professional, you will have the opportunity to work within... ...whole world.
You will be the voice of Regulatory Affairs CMC and you will be responsible for providing scientific and...
...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...
...Category: Regulatory Affairs
Country/Region: DK
Location: Odense, DK... ...have experience in lifecycle management? Then you might be the right... ...Specialist in the Post Approval CMC team.
About the job
As... ..., please contact Department Manager RA LCM CMC Own Sites,...
...Are you experienced within device regulatory affairs and are you passionate about finding new pathways... ...functions, including Research, Device & CMC Development, Clinical, Commercial, and... .... In addition, an ability to think and manage strategically with attention to detail is...
...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...
...technical writing (incl. IP) and/or regulatory submission process and the... ...(ET API MDev) - a part of CMC Chemical Development - and... ...collaboration with Regulatory Affairs.
You will create documentation... ...optimization, and life cycle management. We offer a very interesting...
...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...
...You might be our new Associate Director in one of the Regulatory Affairs CMC & Devices departments in Søborg, Denmark.
The position... ...Your main responsibilities will be focused on:
People management and development
Prioritising and forecasting resource allocation...
...advocacy and partnerships? Then you could be our new Public Affairs Manager for Cardiovascular Diseases. Apply today and join us for a life... ....
Identify and evaluate gaps and needs for the current regulatory and policy landscape in CVD to communicate to regulatory...
...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...
...growing product portfolio and life cycle management activities in Novo Nordisk? Would you like to be part of shaping how we in Regulatory Affairs drive data integrations/migrations... ...will drive activities that enable us to manage regulatory activities across the product...
...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...
...validation documentation from Chemistry, Manufacturing and Control (CMC) analytical departments and contract manufactures (CMOs) in the... ..., we’re life changing.
Contact
For further information, Manager Stine Marie Faaborg at # March 2024
You do not need to attach...
...are looking for a Chemical/Process Engineer to join our team in CMC Chemical Development – a part of CMC API Development. If you are... ...Contact
For further information, please contact Associate Manager, Michael Koch Meldgaard, at 3448 9449
Deadline
May 15th...
...ready to apply your project management experience in an... ...As Analytical Project Manager you will play a key role... ...analytical validations, regulatory documents, submissions to... ...product and drug substance), CMC, Quality Assurance, Regulatory Affairs, and representatives from...
...injectable formulations with-in CMC Drug Product
Ascendis... ...specialist and technical project management skills.
Your key... ...Product Supply.
Writing regulatory quality documentation and support... ...expand in your role, you and your manager will continuously have...
...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...
