MES Lead for API production

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Bagsværd

Do you want to drive change by being at the forefront of modern technology and IT within our Manufacturing and Supply Chain operations? Does your expertise cover handling and leading of Manufacturing Execution System (MES) activities in a GMP regulated production environment? Can you ensure high quality and high customer satisfaction in your daily work?

Then come and joins us as our new MES Lead for API production!

The position
As a MES Lead for API production, you will play a key role in our agile PAS-X project teams and MES system, on a global scale. Our overall aim is to improve the efficiency of all manufacturing-related processes globally. You will be in the center of these transformation activities. As a result, you can expect a dynamic, project-focused community working primarily in Denmark.

The position requires the ability to take independent decisions based on business requirements and business strategy. It influences the quality level of Novo Nordisk’s batch documentation system used in most parts of Product Supply (PS), where you will operate on a high managerial level, enforcing the Novo Nordisk Deployment Model and Target Architecture in projects.

Your responsibilities summed up:
• Oversee new processes and concepts in API: fermentation, freeze drying, material handling,
• Interact with product team for introduction of new PAS-X MES product in API teams
• Drive standardization of MES in API areas by: setting directions to ensure standardization and harmonization on how we implement and deploy the system, ensure compliance/adherence of the technical design and standards are kept, coordination with other MES Area Leads, MES analysts and system architect, quality oversight of all Scrum Teams, compliance - Secure the right documents in place etc. Ready for audit, coaching of project teams - Involvement of more complex tasks
You will be an advisor for G1-G5 approval from content/technical perspective, providing input on how to implement and deploy the system. The job will not always be hands-on – it’s expected that you can guide and communicate around how the harmonized solutions must be implemented.

Qualifications
  • Master’s degree within a relevant discipline e.g., Engineering, business, economics, pharmacist or equivalent
  • Good results working in a similar position
  • Experience with GMP validation of IT systems in a regulated production environment
  • Solid knowledge with MES or other related system (like Syncade or Delta V), GMBR design or PAS-X; experience with production line/equipment integrations is preferred
  • Excellent communication skills in English both written and spoken; Danish skills would be an asset

  • To succeed in this job, you should be able to bridge your technical MES knowledge with local business process requirements to identify and collect data, make a structured analysis and develop excellent standardized and integrated IT solutions in PAS-X. As a person, you’re a strong individual who can come up with innovative solutions and have the ability to demonstrate a capacity for gathering requirements to identify issues, opportunities, and patterns.

    You have a flair for stakeholder management and the ability to be self-motivated, structured, and targeted having a high degree of flexibility. You can use your empathy and IT apprehension to change complex technical challenges and demands into workable solutions. This position requires strong commitment and the ability to make decisions, often in a high-pressure, consensus-driven and political environment. Last but not least, you possess proficient analytical, problem solving and decision-making skills

    About The Department
    Anchored under DD&IT (Digital, Data & IT), Manufacturing IT is the trusted IT partner for our production sites and supply chain colleagues worldwide in Novo Nordisk. The position is based in Denmark at our Headquarters in Bagsværd but with more than 840 colleagues across 7 countries, you will have a global career path and international development opportunities. We will join a truly diverse area with a strong learning culture, flexible working arrangements, and a team that works in an agile and matrix set-up.

    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 Linda Høyer, +45 30791663

    Deadline
    15 August 2023.
    We will interview candidates continually, as we receive the applications.
    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 Bagsværd.

    Jobbet er oprettet på vores service den 4.7.2023, 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.
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    • Bagsværd

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