Sr. Manufacturing Development Scientist, New Drug Products

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Søborg

Could you be looking for an opportunity to play a key role in developing new injectable drug products to treat serious chronic diseases? Want an opportunity to showcase your scientific thinking and collaborative skills? Would you like to work on projects that will potentially change and shape the future of [xxxxx] and offerings for patients worldwide?We are looking for highly skilled scientists to ensure the development of aseptic production processes, centered around the formulation and filling process, suitable for manufacturing sites around the world. If this sounds of interest to you, then you could be our new Scientist / Sr. Scientist based in the Greater Copenhagen area, Denmark. Apply today and join us for a life-changing career.About the department
In Product Supply Aseptic Manufacturing (PS AM), we produce a large portfolio of products fighting serious chronic diseases worldwide.The area New Product Introduction (NPI) is a part of Aseptic Manufacturing Science & Technology (AMSAT) and consists of approximately 90 employees across 4 departments.NPI’s main responsibility is to ensure a smooth transition of [xxxxx] product portfolio into large-scale production and market approval.The position is within the New Manufacturing Processes Omega team, a group of 11 highly skilled employees. The team develops, upscales and implements aseptic production processes (formulation and filling) for new products in the development pipeline. We work in cross-functional project groups but are united to meet team goals and share experience and knowledge.The positionYour main tasks will be:
  • Test activities for introduction of new development products from CMC Development.
  • Spearheading task for test runs and process characterization of formulation and filling process parameters.
  • Leading the process validation activities to prepare and ensure the scope for large-scale market production.

  • You will do this in close collaboration with colleagues within the department and with various stakeholders.Through the job, there will be great opportunities for building a large network, since you’ll be working with both development departments and production sites – [xxxxx]’s own sites, as well as with Contract Manufacturing Organizations (CMOs). Depending on this, you can expect 10-20 travel days a year to primarily EU and US.You will be given the opportunity to work in a professionally challenging setting with a highly engaged and supportive team. We will offer you a creative work environment with great possibilities of developing your professional and personal competences.QualificationsThe ideal candidate has:
  • Minimum M.Sc. degree in Pharmacy, Chemistry, Engineering or other relevant academic area.
  • Relevant experience within formulation and filling in aseptic production/manufacturing within a GMP environment.
  • Experience with Single-Use Systems and extensive knowledge of validation activities.
  • Familiarity with regulatory documentation.
  • Excellent collaboration and communication skills, prioritizing team success above personal achievements.
  • Fluency in spoken and written English.
  • On a personal note, you are self-driven and ambitious, and you are comfortable in a setting with unknowns and several stakeholders, where your actions make a real impact. As you will be working in a changing and complex environment, it is important you are able to adapt, learn and stay in control in challenging situations, with the support of your colleagues. You are quality-minded and have good time-management and planning skills to ensure ambitious deadlines are met. You enjoy working closely in a team to get prioritized tasks completed.Working at [xxxxx]At [xxxxx], 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.

    ContactFor more information, please contact manager, Pernille Theil Bacher on +[xxxxx].
    Deadline27 July 2025Please note, applications will be reviewed, and interviews will be conducted on an ongoing basis, so we encourage you to apply as soon as possible.You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Please assist us in maintaining a fair and inclusive selection process by not attaching a photo to your application.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At [xxxxx] 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 17.6.2025, 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.
    • Øvrige
    • Søborg

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