Are you looking for an opportunity where you can utilize your leadership skills and medical knowledge to generate, interpret and communicate scientific data?
Are you passionate about working with contract manufacturing and thrive in a dynamic, international environment with many stakeholders? Are you ready to be
Do you want to play a key role in accelerating the development of our patient:focused products? Are you passionate about regulatory science and executing on
Do you have experience from either RA, CMC, QA, and/or QC : or any other relevant area? Do you possess a natural interest and flair for regulatory guidelines?
Are you ready to assume a key coordinating role for planning, conduct and follow:up on pharmacovigilance (PV) audits and inspections, working independently
If you are a Quality specialist with a reputation for being a smart quality expert who can handle complex cases with balanced solutions, we want you. Apply now
Are you ready to take on impactful projects and drive the implementation of complex regulatory requirements? Do you have a passion for improving processes and
Global New Product Planning Lead (maternity cover) Are you ready to make an impact by shaping the early:stage Research and Development pipeline and developing
Do you want to play a key role in driving the ongoing safety surveillance activities for early development projects in Novo Nordisk? And would you like to be
Are you a Medical Doctor with an interest in clinical development of pharmaceutical drugs, medical devices and digital health? Would you like to be part of our
Are you passionate about developing user communication solutions that ensure patient safety and support? Do you thrive in a collaborative and diverse
Are you a skilled protein purification professional with a strong interest in optimization and support? Are you excited to work where development meets
Do you want to develop the future standards of aseptic processing (AP) in Novo Nordisk? Does close international collaboration and networking across boundaries
Would you like to join Novo Nordisks dedicated global clinical development team, contributing significantly to ambitious drug development programs? Do you want
Are you an experienced Technical Project Manager with a background in medical device development? Are you ready to take on a leading role in the development of
QC Professional, Biologics Join our QC Biologics team and take part in the journey of restoring brain health. Want to contribute to ensure quality in our
Projects and Partnering Specialist : Projects and Partnering, Global Patient Safety Lundbeck aspires to become a focused innovator developing transformative
evt. med mulighed for deltid (min. 30 timer). Har du interesse for og meget gerne erfaring med Regulatory Affairs – og helt optimalt med Marketing
Do you want to work with policies and regulation on advanced data science capabilities and methodologies ? Do you enjoy working in a fast:changing environment
Are you able to cut through complexity and drive regulatory strategies for high:impact projects? Would you like to work together with experts across multiple