Advanced Process Engineer
19 hours ago
Do you have a passion for Medical Device engineering and a knack for stakeholder management? Are you ready to bring your expertise in assembly or packaging production to a team shaping the future of medical devices? Apply now and join us in Finished Products Manufacturing Science and Technology Manufacturing Development (FPMSAT) to make a difference in global healthcare
The position
As Advanced Process Engineer in the GFPS team, you will work as a very hands-on technical expert, and you will support our global production.
Your primary tasks will consist of, but are not limited to:
- Support all Novo Nordisk finished product sites, including components molding, assembly, and packaging processes for medical devices.
- Ensure products comply with quality and GMP requirements.
- Handle investigations stemming from Customer Complaints.
- See the direct impact of your work on patient safety.
- Interact with varied stakeholders, including Production, Quality, Customer Complaint Centre, Product and Process experts.
The team also trains other Novo Nordisk stakeholders in specific devices where you have the chance to share your knowledge and inspire others about medical device functionality. It is a fast-paced job and equally rewarding as you will see the direct impact of your inputs on the cases and customer complaints we handle in FPMSAT.
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 a proficient user of English, both in writing and orally.
- 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.
- Have an eye for detail for process improvements.
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, able to scope/define the challenge at hand, identify the implications and conclude on the case. 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 to know when you have necessary and sufficient information for decision making. You can prioritize, are good at completing your tasks in time and move on to new tasks with energy and enthusiasm.
About the department
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 FPMSAT, 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.
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.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for a 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
If you have any questions about the position, please don’t hesitate to reach Sudeep Desai at ( ) +45 30796473.
Deadline
21.01.2025
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.
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