• Job Description

  Req#: 294255

  Are you passionate about innovation and skilled in stakeholder management? Do you thrive in a dynamic environment and have experience in Assembly and/or Packaging production? If you're ready to work with cutting-edge medical devices and apply you knowledge and experience to secure product quality, then you could be the perfect fit for us. Apply now and be part of shaping the future of healthcare technology!

  We are searching for a passionate and skilled Advanced Process Engineer in Global Finished Product Support (GFPS) in Device Manufacturing Development (DMD).

  The position

  As our new Advanced Process Engineer, you will work as a very hands-on technical expert, and you will support our global production. You will play a key role in supporting all Novo Nordisk finished products sites - from components moulding, assembly, and packaging processes of our medical devices. We do this to secure that our products comply with quality and GMP requirements.

  In addition, you will handle investigations from Customer Complaints where you can feel the direct impact of your work for the end patients. You will interact with a varied group of stakeholders – Production, Quality, Customer Complaint Centre, Product and Process experts being the key ones. Moreover, the team trains other Novo Nordisk stakeholders in specific devices, which allows you to share your knowledge and inspire others about medical device functionality.

  Qualifications

  
  To thrive in this role, we envision you as someone who:

  
  • Has minimum 2 years of relevant experience.
  • Holds a Master’s degree within engineering, pharmaceuticals, or a similar field.
  • Has good GMP knowledge and a strong quality mindset.
  • Is fully proficient in written and spoken English.
  • Has excellent interpersonal and communicative skills, which enable you to build credibility and engage stakeholders at all levels.

  While not a prerequisite for applying for the position, we put together a list of skills that we consider advantageous. You will stand out if you:

  
  • Have experience in manufacturing preferably within moulding, assembly or packaging of Novo Nordisk devices, however other production experience in high regulation industries will also be considered.
  • Are familiar with 2D/3D scans, statistics, probability and are familiar with requirements of working medical devices.
  • Are an effective communicator for writing concise memos and conducting classroom training.
  • Can develop and improve processes with case handling and stakeholder interaction.

  On a personal level, you thrive in a busy environment with an unpredictable workday, and you enjoy taking on new challenges. You are an analytical problem solver, with the ability to scope/define the challenge at hand, and to identify the implications, and to conclude on the given cases.
  

  You are service minded towards the stakeholders, but also confident to challenge them to secure best quality towards patients. You never compromise on quality, at the same time, you are pragmatic and know when you have the necessary and sufficient information for decision making. You can prioritise, are good at completing your tasks in time, and move on to new tasks with energy and enthusiasm.

  About your new team: diverse, supportive, dedicated

  You will join the GFPS team, a dedicated and highly competent team, which is a part of the Product Control and Global Support department in DMD, physically located on our site in Hillerød. The team works at the crossroad between Devices & Delivery Solutions (R&D), Manufacturing Development, Quality and Production. Our field of expertise covers extensive device knowledge down to a component level, risk assessment, understanding of assembly and packing process, test methods, and operational principles.

  We are a diverse team, with both men and women, internationals, as well as Danes, with different levels of experience in our fields. We like internal collaboration on cases to ensure consistency towards our stakeholders. Although our work is demanding and fast-paced, we also try to keep an informal tone and a pleasant atmosphere. You will be a fully-fledged member of the team from day one and you can rely on us to welcome and onboard you properly.

  What do we do?

  The main task for the team is to provide expert input on the impact of defects at product- and patient level. Furthermore, the team is responsible for conducting expert investigations of technical customer complaints related particularly to the FlexPen, FlexTouch and Single Dose device platforms aiming to clarify the impact of any potential error. With the extensive knowledge anchored in these device platforms, the team also develops training material and conducts device training across the organization. With a well-defined set-up for FlexPen and FlexTouch delivery platforms, the team is also developing maturity on the Single Dose Device (SDD) and NovoPen device platforms.

  Contact

  
  If you have any questions about the position, please don’t hesitate to reach Sudeep Desai at (SUDE@novonordisk.com) +45 30796473.
  

  Deadline

  
  25 February, 2024. Please note that applications will be reviewed continuously, and interviews may be initiated prior to the deadline.

  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.

• About the company

  Novo Nordisk A/S is a Danish multinational pharmaceutical company headquartered in Bagsværd, Denmark, with production facilities in eight countries, and affiliates or offices in 5 countries.

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