Would you like to contribute to our ambition of a fully integrated and highly automated facility? This is your opportunity to be involved in a new, high-profile greenfield project, and to be involved in shaping a new department. It is our ambition to achieve Instant Release of our products by real-time quality control and release by exception, and integration and digitalization is therefore of crucial importance. We are looking for an Integration Manager to lead the project tasks related to integration between MES and SAP. Apply today and join us for a life-changing career! The position In Biotech & Rare Disease (BRD) we are planning to expand our production facilities in Hillerød, Denmark, to meet the future needs of our growing product pipeline. Our MES system, PAS-X, must be integrated to the central SAP system, to ensure transaction of material consumptions, traceability etc. You will be working in an international working environment, driving the tasks related to the SAP integration including development of a SAP Batchmodel, identifying SAP Meta data in close collaboration with Automation, Process-responsible, QA and our core SAP Teams. The assignment will also include building up a local SAP team, that beside executing a successful integration also will prepare for tasks related to operation, including product changes and thereby new SAP batch models and metadata updates. You will play a central role in maintaining and optimizing our interface configurations while ensuring the stability and support of our production. In this position, you will primarily work with interfaces between different IT systems, including SAP (SAP ECC and SAP EWM), PAS-X & DeltaV. Your main responsibilities will be:

Drive the local integration of PAS-X to the central SAP ECC and SAP EWM (Enhanced Warehouse Mgmt.)

Development of SAP batch models in close collaboration with Automation- and Process responsible.

Plan workshops to identify meta data for SAP.

Contribute to the efficient execution of our manufacturing processes during hyper-care period after project ends, and the facility enters production.

Development of a small local SAP team, that will be responsible for the different SAP Batchmodels, update of Meta data, handling of deviation related to local integration to SAP ECC.

Work in close collaboration with the PAS-X team and understanding of the mechanics of the between PAS-X, SAP-ECC & DeltaV

As part of your key duties, you will also learn about the PAS-X system in order to improve the integration and future optimizations. Qualifications We welcome a candidate with experience and knowledge within technical or IT Project implementations in a production context with a very high level of automation and integration between systems. To succeed in this role, we expect you to also have:

A background in engineering, automation or other relevant fields for this position, preferably an academical background, however we value experience most.

High level of business and process understanding.

Experience in a regulated and automated production environment and experience with one or preferably more of the following: Automation, Digitalisation, and Integration will also be advantageous.

Experience from working within production support, preferably knowledge of API in a GMP-regulated environment. Preferable experience with validation/qualification.

General knowledge of API processes, MES (Manufacturing Executing System) systems, DCS (Distributed Control system) systems.

Fluent in English, both oral and written.

On a professional level we also expect you to have a structured working approach and high data quality mindset as well as excellent people skills and a proven record of collaborating with stakeholders on all levels. As a person, you enjoy collaborating, learning, and sharing information with others. You are driven by achieving great results together with colleagues. This drives you to be close to the manufacturing processes and everyday lives of your stakeholders as you are curious to learn and understand how IT & Automation can help improve the production processes. About the department Our team is part of the BRD Active Pharmaceutical Ingredient (API) Denmark Area located in Gentofte, Hillerød and Kalundborg. This is where the active ingredients, going into all our life-saving biotech products, are made by app. 500 committed colleagues. We manufacture through complex chemical and biotechnological processes (this includes cultivation, recovery, purification, and freeze-drying), which requires a high level of expertise, commitment, and engagement from our employees. We are producing at full speed in existing facilities while building and ramping up new state-of-the-art additions to keep up with demand and new Novo Nordisk products. We bring value to patients by delivering the purest possible high-quality API made in compliance with GMP. We drive change by always looking for improvements within our processes, and in the way we work together to make our products reach as many patients as possible. Working at BRD, Novo Nordisk BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases but also using our competencies in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2650 colleagues committed to driving change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – but we also strive to make a difference for our employees by promoting a learning culture with a high level of trust, innovation, and development for everyone. Are you ready for a life-changing career? Contact For further information, please contact Senior Project Manager, Michael Saaby +45 30 79 91 66, Director Helle Grubbe at +45 34 48 11 29 Deadline 27 August 2023. We will review applications and conduct interviews 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 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 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.