(Senior) Analytical Project Manager

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Måløv

Are you ready to take charge and make an impact on a range of early and late-stage drug product development projects? Are you prepared to leverage your project management expertise and analytical development skills in a dynamic organization where you'll be pushed to grow and expand your capabilities to the fullest? Do you seek to join a vibrant and highly skilled analytical project team? We are searching for Seasoned Analytical Project Managers to bolster our diverse development portfolio. We lead analytical development across a variety of platforms, molecule sizes and types within drug substance development, and injectable and oral drug products. If you possess the relevant project management and analytical development skills, apply now and step into a challenging and rewarding opportunity. The position You will interact with a wide variety of stakeholders such as Analytical departments, other CMC project managers, Production/Pilot, Quality Assurance and Regulatory Affairs. As Analytical Project Manager you will be responsible for:
  • Overseeing project management of analytical development and characterization activities and analytical strategies related to drug substance and drug product

  • Guiding projects through different stages of clinical development in collaboration with a broad range of stakehokders, such as Global Research, Product Supply and contract manufacturers

  • Leading the analytical project team in a compelling and inspiring manner incl. the development of regulatory applications and various internal and external documents

  • 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

    • You will be a member of the CMC Project Core Team, where you will be responsible for planning and coordinating development activities within your area of expertise and ensuring deliveries. 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

    • In addition, you are results-driven, taking pride in meeting milestones and inspiring your colleagues with a positive, proactive attitude. You excel in independent work while also being inclined to collaborate with colleagues and stakeholders across various functions and departments. This position may require travel, especially in relation to potential CMO collaborations. The amount of travel will vary based on assigned projects but is anticipated to be around 5-10 days per year. Additionally, while we welcome candidates of all nationalities, the majority of the work will be based in and out of Denmark, necessitating a willingness to relocate to Denmark. About the department As part of Novo Nordisk PSQIT organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a “can do” mind-set. 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 18 August 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.


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    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 14.5.2024, men kan have været deaktiveret og genaktiveret igen.

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