Regulatory Affairs CMC Expert (Small molecules, Early and Late development projects)
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We are expanding our product and project pipeline in Novo Nordisk and are looking for an engaged RA CMC Specialist with expertise in small molecules to join RA CMC Biotech & Rare Disease (BRD) in Novo Nordisk Global Regulatory Affairs unit. If you are curious about drug development within Rare and Other Serious Chronic Diseases, willing to take lead, set strategic direction in projects and be a regulatory affairs expert in a growing organization- then this might be the job you are looking for. The position(s) As a Regulatory CMC Specialist, you will act as RA CMC lead for small molecule projects in early and late-development and are expected to drive scientific and regulatory discussion across our portfolio. You will be working closely together with decision-makers across multiple functions in a global environment, you thrive with the challenging reality of international communication across time zones, cultures, and circumstances. You will build partnerships with key Stakeholders from other functions internally as well as external partners. You will also provide Strategic, tactical, and operational regulatory input to projects. In addition, you will also be responsible for and contribute to the success of RA CMC BRD by:
Applying regulatory intelligence and establish strategy for submission of Clinical trial applications and Marketing authorisation Drive submission of regulatory files, response to questions from health authorities Ensuring compilation, review and submission of pre-meeting packages for authority meetings; conducting rehearsals and participate in meetings Addressing dilemmas and analyse complex challenges to propose new ways to support projects with regulatory expertise Facilitating the regulatory approval process by identifying key risks and ensure timely, complete and high-quality answers to authority questions Contributing to improvement projects The role requires the ability to work effectively with people from different functions and organisational levels, calling for high cultural awareness and the necessary skills to encourage and influence colleagues, governance, and key stakeholders. Our commitment to innovation also applies to the way we work: We embrace remote work and the hybrid workplace. Whether you prefer to work from home, at the office or to blend the two to your liking. Qualifications
You hold a Master and/or Ph.D. degree in life sciences. You have acquired solid Regulatory CMC experience either from the pharmaceutical industry or from a health authority. We imagine that you have minimum 4-8 years of experience with above and have hands-on experience with small molecules and/or synthetics and within several of the areas below: Extensive experience working with small molecules Broad understanding of global drug development In-depth knowledge of regulatory requirements for CTA’s and/or NDA’s/BLA’s Extensive global regulatory experience in obtaining product licenses in the EU, US and other major countries Experience of interacting with key regulatory authorities e.g. FDA, EMA, PMDA, and scientific advisory meetings Experience of navigating within an environment of tight timelines, high-complexity, non-standards and diverse tasks in known and new therapy areas Excellent analytical skills, systematic approach to identify root causes and propose innovative ways to solve problems Ability to communicate complex scientific procedures with technical proficiency both orally and in writing. Advanced level written and spoken English is a prerequisite As all work takes place in multidisciplinary project groups, we expect you to be a dedicated team player, find it easy to build working relationships, and gain recognition amongst stakeholders with your proactiveness, integrity, and communication skills. About the department
Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring fast regulatory submissions and approvals in all our global markets. In RA CMC Biotech & Rare Disease we are a group of 45 highly skilled and dedicated regulatory professionals divided into three departments and involved in every Regulatory CMC aspect concerning our Rare and Other Serious Chronic Disease products. The project portfolio is rapidly growing; therefore, we are looking for a Regulatory Expert to join us and work on small molecule projects. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re 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’re all working to move the needle on patient care. Contact For more information on this role, please contact Ana Mora Agudo +45 3075 0292. Deadline for application
08th May 2023 Candidates will be evaluated and interviewed on an ongoing basis, so do apply at the earliest. Please submit an English version of your resume and include a few sentences about your motivation towards this position. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Should you wish to learn more about working at Novo Nordisk, here may be a good place for you to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html 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.
You hold a Master and/or Ph.D. degree in life sciences. You have acquired solid Regulatory CMC experience either from the pharmaceutical industry or from a health authority. We imagine that you have minimum 4-8 years of experience with above and have hands-on experience with small molecules and/or synthetics and within several of the areas below:
Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring fast regulatory submissions and approvals in all our global markets. In RA CMC Biotech & Rare Disease we are a group of 45 highly skilled and dedicated regulatory professionals divided into three departments and involved in every Regulatory CMC aspect concerning our Rare and Other Serious Chronic Disease products. The project portfolio is rapidly growing; therefore, we are looking for a Regulatory Expert to join us and work on small molecule projects. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re 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’re all working to move the needle on patient care. Contact For more information on this role, please contact Ana Mora Agudo +45 3075 0292. Deadline for application
08th May 2023 Candidates will be evaluated and interviewed on an ongoing basis, so do apply at the earliest. Please submit an English version of your resume and include a few sentences about your motivation towards this position. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Should you wish to learn more about working at Novo Nordisk, here may be a good place for you to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html 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 "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 18.4.2023, 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.
- Øvrige
- Søborg
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