(Senior) Analytical Project Manager
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Måløv
Do you want to drive and impact a variety of early and late-stage drug product development projects? Are you ready to apply your project management experience and analytical development skills in an exciting organization, where you will get challenged, grow, and expand your capabilities to the fullest? And do you want to join a dynamic and highly competent analytical project team? We are looking for multiple Experienced Analytical Project Managers, at Principal Scientist/specialist level, to support within various fields of our development portfolio. Could be within molecular biology techniques, small/large molecules and/or oral/injectable drug products. Apply now if you have the relevant project management and analytical development skills. The position You will interact with a wide variety of stakeholders such as Analytical departments, Production, Quality Assurance and Regulatory Affairs. As (Senior) Analytical Project Manager you will be responsible for: Analytical development and characterization activities and strategies for drug substance and drug product, through project management Driving the projects through the different stages of clinical development and collaborate within CMC Development and with our colleagues in Product Supply as well as other areas of the R&D organization or contract manufacturers Leading the analytical project team in an engaging and motivating way and participate in writing and compiling regulatory applications and various internal and external documentation Coordinating the transfer of analytical methods from our research unit to CMC Development & Scaling and further on to our manufacturing unit Product Supply or to a contract manufacturer Communicating and coordinating with stakeholders within and outside CMC Development Apart from that, you will be a member of the CMC Project Core Team where you will be responsible for planning and coordinating development activities within your expertise area and ensure deliveries according to the project plan. Qualifications You will be a great asset to our department because you have: Extensive experience in leading analytical activities in either early phase and/or late phase clinical development. Experience in managing and executing smaller and larger projects. Scientific experience within analytical development, experience with regulatory submissions and perhaps experience in working with Contract Manufacturing Organisation (CMO). A relevant academic degree within Pharmacy, Chemistry, Biology, Engineering, or a similar field. Full professional proficiency in English Have a high level of energy to drive activities and engage your colleagues forward Apart from that you are result-oriented, take pride in delivering on your milestones, and motivate your colleagues with a positive, forthcoming attitude. You work well independently, although you should also be motivated to cooperate with colleagues and stakeholders across functions and departments. Travel may occur in this role e.g. in relation to CMO collaborations. Will depend on assigned projects but expected 5-15 days per year. About the department Your new department, CMC Drug Product & Analytical Development - Project Office, consists of app. 50 employees located in Måløv. The department is involved in early and late-stage drug product development, analytical development and chemical and biological characterization of new entities moving through the clinical phases of drug product development. 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 further information, please contact Senior Manager Taus Laurent Meincke at [email protected] Deadline 8 April 2024. Applications will be reviewed continuously, and interviews will be conducted during the posing period, so please do not hesitate to apply. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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. 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 "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 14.2.2024, 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.
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