Drug Product Manager
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Søborg
Do you enjoy working in an environment where your actions have real impact? And would you like to be part of a team that pushes the boundaries for project management and product development in the pharmaceutical industry?At our patients and their needs are always front and center. With increased demand for ’s products, we will both lead development of new drug products and development of new and more effective ways of producing and delivering them. If you would like to be a part of this journey, we offer an exciting drug product project manager position in New Product Introduction (NPI)!The positionAs part of AMSAT (Aseptic Manufacturing Science and Technology), the purpose of NPI is to deliver well established and robust processes to manufacturing to ensure smooth product introduction and launch. To succeed with this, NPI project managers need to have a strong focus on building project teams and promoting a dynamic learning culture where close collaboration and openness are hallmarks.The Drug Product Sciences department (DPISO) consists of three teams: A team of project managers, a team of process responsible scientists and a team of product responsible scientists. The drug product managers have the responsibility to coordinate all activities related to scale up of formulation and filling, process validation, and development of submission documents to authorities.As an NPI Drug Product Manager you will serve as Product Supply’s representative in core groups and cross-functional teams and lead internal activities in our project teams. The projects have a very high level of complexity both technically and in terms of stakeholder landscape and strategy. Moreover, the highly regulated pharmaceutical GMP environment creates a particular set of challenges that we need to handle effectively to secure patient safety.Your daily tasks (among others) are:Work closely together with stakeholders locally in NPI, with colleagues in CMC, manufacturing sites and other areas across or with external partners Maintain the overview of your project, set the direction for the team and ensure that deliverables are met, and strategies are executed Secure timely development of transparent project plans and communication of these to stakeholders Develop how we do Project Management in NPI to succeed with current and future projects Your qualificationsAn academic degree of at least BSc level within Life Science or engineering (e.g. Pharmacology, Biochemistry, Biology or Medicine) 5+ years of experience working with project management within the pharmaceutical industry, or extensive experience from late-stage drug development product projects. This experience could be within development, production, or other relevant disciplines You are assertive and have strong leadership and interpersonal skills, coupled with a good sense of diplomacy; all to enable progress in a complex stakeholder landscape You are self-driven and independent, and inspire and energize your team and your colleagues, set clear and ambitious goals, and work closely together with your stakeholders to reach our goals Fluency in English is a must for this position
As a person, you can work in a high paced and dynamic environment. You prioritize and create transparency for your project, ensuring that you keep the overview and share it with your team members. You have excellent communication skills to all levels in the organization. Based on project progress and decisions you can through uncertainty to rapidly develop- and clearly communicate scenarios, impact of risks and recommendations to the decision makers.About the departmentIn AMSAT we produce a large portfolio of products fighting serious chronic diseases worldwide. New Product Introduction consists of 100+ employees across 4 departments situated in Søborg, Denmark. The main responsibility of the department is the transition of development products into large scale manufacturing and market approval. This includes production design, material and process sciences, product stability and coordination of production for late-phase clinical trials.Working at At we strive for excellence. As a world leader in diabetes care and a major player in hemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.ContactFor further information you are welcome to contact Director Sussie Steen Jensen + . This contact shall cover questions about the role – be advised it will not support queries about your recruitment status.Deadline22 April 2025
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 to your CV and submit it in English.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At 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.
As a person, you can work in a high paced and dynamic environment. You prioritize and create transparency for your project, ensuring that you keep the overview and share it with your team members. You have excellent communication skills to all levels in the organization. Based on project progress and decisions you can through uncertainty to rapidly develop- and clearly communicate scenarios, impact of risks and recommendations to the decision makers.About the departmentIn AMSAT we produce a large portfolio of products fighting serious chronic diseases worldwide. New Product Introduction consists of 100+ employees across 4 departments situated in Søborg, Denmark. The main responsibility of the department is the transition of development products into large scale manufacturing and market approval. This includes production design, material and process sciences, product stability and coordination of production for late-phase clinical trials.Working at At we strive for excellence. As a world leader in diabetes care and a major player in hemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.ContactFor further information you are welcome to contact Director Sussie Steen Jensen + . This contact shall cover questions about the role – be advised it will not support queries about your recruitment status.Deadline22 April 2025
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 to your CV and submit it in English.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At 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 1.4.2025, 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.
- 01.04.2025
- Øvrige
- Søborg
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