API Technical Project Manager
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Søborg
Do you want to use your professional expertise within organic chemistry, Active Pharmaceutical Ingredient (API) process development and/or manufacturing to drive and impact a variety of early and late-stage development projects? In that case, you could be our new API Technical Project Manager in the API Project Office. Apply today! The position You will coordinate and lead all CMC API project activities through the different stages of clinical development, from Lead Candidate Selection to final regulatory approval, primarily for projects within synthetic organic chemistry, e.g., peptide, small molecule, or semi-recombinant APIs. Using your technical expertise, you will coordinate process development activities performed in our laboratories or outsourced to a Contract Manufacturing Organization (CMO) - this will typically include synthesis (e.g., by solid-phase peptide synthesis or organic synthesis), purification and drying manufacturing steps. The CMC API activities will also include establishment of new API starting materials, planning of pilot scale manufacturing, development of upscaling for full scale manufacturing, authoring of regulatory documentation including Clinical Trials Application (CTA) and New Drug Application (NDA) as well as writing and compiling of various internal and external documentation. As an API Technical Project Manager, you will be a member of a CMC Project Core Team and you will lead a sub-project team of subject matter experts focused on the API Development in an engaging and motivating way. The position will also give you the opportunity to collaborate with cross-functional stakeholders within CMC Development and coordinate the transfer of project activities from our research unit to CMC Development and eventually to our Product Supply manufacturing unit or to a CMO. Qualifications As a minimum you have a M.Sc. in chemistry, organic synthesis, chemical engineering, or another relevant field within pharmaceutical sciences. A Ph.D. in synthetic organic chemistry and specific knowledge within peptide synthesis will be a clear advantage. The preferred candidate has: Minimum 5 years of experience working with API process development and/or manufacturing in GxP regulated facilities Experience working with external contract manufacturers is a benefit Experience with project management in a multidisciplinary organization is required, including cross-functional communication and stakeholder management, project planning, risk management, and deliverable tracking. The ability to manage competing timelines and priorities Strong problem-solving and organizational skills Excellent written and verbal communication skills with expert proficiency level using Microsoft Word, Excel, and PowerPoint You have a high level of energy to drive your projects and engage your colleagues. You are result-oriented and take pride in delivering on your milestones, and you motivate your colleagues with a positive, forthcoming attitude. You can function independently as well as in a team-based environment. You must have fluency in written and spoken English. Options to learn the Danish language are available. About the department CMC API Project Office is part of Chemistry, Manufacturing & Control (CMC) API Development and consists of approximately 20 highly skilled and motivated employees located in Bagsværd, Denmark. The department is involved in the entire CMC API portfolio of development projects moving through the clinical phases from early to late-stage API development and production of new synthetic, semi-recombinant or recombinant API candidates. We strive to have a high level of scientific knowledge and a helpful and pleasant working environment About 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 Jens Engel-Andreasen, Project Manager +45 30790012 or Mads Holger Rønnest, Associate Manager +45 30777701. Deadline 27 October 2023 We will review applications and perform interviews on an ongoing basis, so you are encouraged to apply as soon as possible. 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 "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 5.10.2023, 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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