Advanced Process Engineer
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Hillerød
We are searching for a passionate and skilled Advanced Process Engineer in Global Finished Product Support (GFPS) in Device Manufacturing Development (DMD) – could that be you? With experience from Assembly and/or Packaging production and a desire to work with some of the most cutting-edge medical devices, you may be exactly who we need. Apply today! The position If you have flair for teaching others about medical devices and their functionality and can ensure that process reliability goes hand in hand with a strong quality focus, then we invite you to read further. 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. You play a key role in supporting the moulding, assembly, and packaging processes of our medical devices. We do this to secure our products comply with quality and GMP requirements. You will interact with a varied group of stakeholders – Production, Quality, Product and Process experts being the key ones. 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 receive in DMD. The seniority of the position will be adjusted as per the candidate experience. Qualifications
To thrive in this role, we envision you as someone who:
• 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:
• you have a minimum of 1-3 years of 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, able to scope/define the challenge at hand, identify the implications and able to conclude on the case. You are service minded towards the stakeholders but can also secure to challenge them to secure best quality towards patients. You never compromise on quality; at the same time, you 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 Who will you be working alongside with? 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. 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 and FlexTouch family devices aiming to clarify the impact of any potential error. With the extensive knowledge anchored in the team on FlexPen and FlexTouch device family, 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 in the Single Dose Device (SDD) and NovoPen family of devices. Contact
If you have any questions about the position, please don’t hesitate to reach Sudeep Desai at ([email protected]) or +45 30796473.
Deadline
27 December, 2023. 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.
To thrive in this role, we envision you as someone who:
• 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:
• you have a minimum of 1-3 years of 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, able to scope/define the challenge at hand, identify the implications and able to conclude on the case. You are service minded towards the stakeholders but can also secure to challenge them to secure best quality towards patients. You never compromise on quality; at the same time, you 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 Who will you be working alongside with? 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. 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 and FlexTouch family devices aiming to clarify the impact of any potential error. With the extensive knowledge anchored in the team on FlexPen and FlexTouch device family, 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 in the Single Dose Device (SDD) and NovoPen family of devices. Contact
If you have any questions about the position, please don’t hesitate to reach Sudeep Desai at ([email protected]) or +45 30796473.
Deadline
27 December, 2023. 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Hillerød.
Jobbet er oprettet på vores service den 27.11.2023, 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.
- Øvrige
- Hillerød
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