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...Are you able to cut through complexity and drive regulatory strategies for high-impact projects? Would you like to work together... ...functions in a global environment?
Then join Global Regulatory Affairs in Novo Nordisk and be our new Senior Regulatory Professional...
...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...
...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...
...high professional competency and leadership experience? If so, we have an opportunity for you. We are currently seeking a Manager to lead our CMC OP Dev CMO QA team (Chemistry, Manufacturing and Control, Oral Product Development, Contract Manufacturing Organizations) in...
...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...
...join Ascendis Pharma as our new Senior Regulatory Operations Manager.
Ascendis Pharma is a fast-growing... ....
Collaborating with Regulatory Affairs and contributing functional areas to create... ...documents in all disciplines (e.g., CMC, nonclinical, clinical, and regulatory...
...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...
...matter expert and local point of contact for activities supporting Regulatory submissions, site activation and maintenance for awarded... ...you will bring to the role
Strong organizational and management skills. Strong planning, strategizing, managing, monitoring, scheduling...
Fjernjob
...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...
...Biologics Production, CMC Biologics
Are you... ...commercial production.
Managing and working closely... ...fulfilling quality and regulatory expectations.
Work close... ...QA, QC, Regulatory affairs, Supply chain and finance... ...planning own work.
Manages ambiguity and thrives in...
...We are rapidly expanding our product and project pipeline in Novo Nordisk and are looking for experienced Regulatory Affairs CMC Experts to join RA CMC & Device , Diabetes and Obesity, a part of Novo Nordisk's Development organization.
If you are passionate...
...interested in learning how Novo Nordisk works with government affairs on the headquarters (HQ) level? If so, join us as our talented... ...Through this position, you can strengthen your skills in project management, stakeholder engagement, and public affairs.
Your...
...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...
...validation documentation from Chemistry, Manufacturing and Control (CMC) analytical departments and contract manufactures (CMOs) in the... ....
Contact
For further information, please contact Manager Stine Marie Faaborg at ****@*****.***
Deadline...
...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...
...role where you can directly contribute to how data flows and regulatory is handled at the fastest growing Digital Bank in the Nordics.... ...streamlined reporting, enhancing compliance and strategic financial management.
Main Responsibilities, and typical day to day
You own...
...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...
...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...
