RA CMC Expert for Biotech and Rare Disease Area
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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, Biotech and Rare Disease, a part of Novo Nordisk's Development organization. If you are passionate about drug development and want to be a subject matter expert in a leading international organization, then this might be the job for you. You will have the opportunity to take the lead and set the strategic direction in projects of crucial importance to Novo Nordisk’s patients on a global level. Apply now for a life-changing career! About the department Novo Nordisk Regulatory Affairs CMC & Device makes medicine available to patients around the world by ensuring fast regulatory submissions and approvals in all our global markets. The RA CMC Biotech and Rare Disease area consists of approx. 40 highly skilled, dedicated colleagues with very diverse backgrounds and experience, who are involved in every Regulatory CMC aspect concerning products and projects in these areas. As Novo Nordisk’s product portfolio is growing, we are developing and implementing highly diverse CMC solutions to the complex manufacturing processes, therefore we are looking to expand our team of experts within RA CMC. Visit our Regulatory Affairs Careers webpages For more information about job content and qualifications, please visit the Novo Nordisk Regulatory Affairs Careers webpages at https://www.novonordisk.com/careers/career-areas/research-and-development/regulatory-affairs-careers.html The position As a RA CMC Expert, you will have the opportunity to work within late-stage development, preparing for upcoming MAA/NDA/BLA submissions and roll out in the whole world. You will be the voice of Regulatory Affairs CMC and you will be responsible for providing scientific and strategic input to the projects you work with to obtain the regulatory approvals. You will turn your knowledge within pharmaceutical operations into regulatory pathways and develop global regulatory CMC strategies based on current legislation and regulations. You will be in the centre of project planning and execution – responsible for planning, coordinating, and reviewing regulatory documentation related to the drug e.g., supporting preparation of applicable sections of submission packages, responses to agency questions for global markets and agency meeting packages. More specifically, you will be accountable for: Planning, executing and driving strategic regulatory CMC activities Applying CMC regulatory intelligence to develop robust regulatory strategies Identifying as well as improving regulatory CMC practices, processes and approaches related to regulatory CMC documentation and strategies Our commitment to innovation also applies to the way we work. We therefore embrace the hybrid workplace – with a blend of home office and on-site work preferably in Søborg, Denmark where the global RA CMC & Device department is based. Qualifications You come with a strong scientific and technical background and mindset, which you have acquired through your extensive experience with RA CMC and/or pharmaceutical operations – manufacturing, product supply, process development, CMC development, analytics, quality assurance and other related areas. The ideal candidate should have: Master’s degree and/or PhD in a relevant field At least 5 years of relevant experience within RA and/or pharmaceutical industry. High proficiency in English - written as well as spoken. Great communication skills as all work takes place in multidisciplinary project groups. You are a dedicated team player, you find it easy to build working relationships, and gain recognition amongst stakeholders with your proactiveness and integrity. Furthermore, you thrive in the challenging reality of international communication across time zones and cultures. Working at Novo Nordisk At Novo Nordisk, we do not wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we are all working to move the needle on patient care. Contact For more information regarding the role, you are welcome to contact Dorte Lunøe (+45-30790217) or Nermin Ipek (+45-30790261). Deadline 20 March 2024. If you are interested in this role, please apply as soon as possible. Applications will be evaluated on an ongoing basis, so there may go some time before you hear from us. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 21.2.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Apoteker
- Søborg
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