Senior Quality Management System Professional in Emerging Technologies

Måløv

Are you passionate about quality and want to help build, improve, and maintain the Quality Management System (QMS) for our newly established Process Analytical Technology (PAT) Department?
Do you want to set the standard and strategy for the quality level of PAT solutions as part of the control strategy for our Oral Product portfolio in Emerging Technologies (ET)?
If so, here is a unique job opportunity with great colleagues waiting for you!
The Position
  • As a Senior Quality Professional in our PAT Department, you will play a crucial role in driving and implementing GMP projects, focusing on building the foundation of PAT QMS. Your responsibilities will include:

  • Taking an active part in setting the strategic QMS direction for PAT in Novo Nordisk and building up the global structure for QMS PAT.

  • Collaborating with peer QMS partners to ensure alignment and consistency in quality standards.

  • Contributing to process improvement and driving projects to enhance efficiency and effectiveness.

  • Ensuring compliance with regulatory standards and internal quality requirements.

  • Building and maintaining strong relationships with stakeholders across the organization, mapping the interlink to QMS areas of Quality Control, Manufacturing Development, and Production

  • Qualifications
    To succeed in this role, you should have:
  • Hold an academic degree, preferably in Engineering, Pharmacy, Chemistry, Biology, Biopharmaceutics, or a related field, along with a minimum of 3-5 years of relevant work experience in the medical device or pharmaceutical industry. This experience should be particularly focused on areas such as QMS, Quality Control, production, or similar functions.

  • Demonstrate experience in driving or participating in projects and process improvement initiatives.

  • Exhibit a high level of proficiency in both written and spoken English, with proficiency in Danish considered advantageous.

  • Possess excellent stakeholder management skills.

  • While not mandatory, it would be beneficial to have experience in production and QC, as we are transitioning our developed methods into both QC and production.

  • As a person, you possess a strong quality-oriented, proactive, and pragmatic mindset, with the ability to thrive in fast-paced environments. We're looking for someone who enjoys working with people from different professional backgrounds and is excited to work in a dynamic environment where things are always progressing. If you're eager to be a part of a team that's making a difference and pushing boundaries, then we want you to join us! About the department
    The position is part of the PAT department in Oral Product Development, which is part of Novo Nordisk's oral solid dosage units. The department's ambition is to develop world-class tablet products for patients living with chronic diseases, including obesity, diabetes, and any future oral solid dosage treatment for other diseases.
    The department currently consists of four teams that work together to develop and implement new PAT applications for the oral drug product pipeline.
    Each team has a specific responsibility:
  • Team 1 focuses on early development, Proof of Concept, and scouting for new PAT applications.

  • Team 2 is responsible for developing PAT methods for specific drug products.

  • Team 3 validates and implements the PAT methods for commercial application.

  • Team 4 manages the overall portfolio of PAT projects in Oral Product Development.

  • As the Senior QMS professional in the department, you will be covering GMP and compliance activities for all teams, covering the entire development from early scouting to final transfer to market production and QC.
    Working at Novo Nordisk
    At Novo Nordisk, we don’t wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
    Contact
    For further information, please contact hiring manager Mélanie Carpin, +45 30 79 59 97, [email protected]. Deadline
    5 June 2024 We will review applications on an ongoing basis, so we encourage you to apply as soon as possible.
    To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
    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 Måløv.

    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Øvrige
    • Måløv