Design Control & Quality Associate, Secondary Packaging
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Hillerød
Do you see the uncovering of risks and defining robust packaging designs for pharmaceutical production as an exciting discipline? Do want to gain experience in a cross discipline between Design Control and Quality Specification for packed products and printed packaging materials in a supporting and learning role? Would you like to join a team which supports the entire range of Novo Nordisk secondary packaging solution? If yes, you could be the profile we are looking for as Design Control & Quality Associate.
The position
In the role of Design Control & Quality Associate in Secondary Pack Maintenance you will function as a supporting element with own portfolio of tasks and responsibilities for assessing severity of identified risk and define requirements for our production lines to ensure patient safety and product quality. Further, you will be part of the product responsible team who ensures proper transfer of new developed products from our R&D division to the marketed portfolio of Device Manufacturing Development (DMD).
In Device Manufacturing Development (DMD), Secondary Pack Maintenance we own and maintain specifications for Novo Nordisk secondary packaging.
You can look forward to a position where your work has a high impact on the packaging of the products that reach the patients. The job will give you a great opportunity for working with innovative products on an international level and for having a broad range of contacts including production sites globally, sourcing & supply chain, R&D, Quality Assurance, regulatory affairs, customer service and affiliates.
Qualifications
• You might recently have graduated but you hold minimum a bachelor’s degree within engineering, natural sciences, or similar.
• Experience from working in or with a highly regulated industry, e.g. medico or pharmaceuticals, automotive or aerospace is a plus but not a prerequisite.
• You are very attentive to details and have a natural understanding of procedures and why these are important in a regulated industry.
• You are eager to learn and you reflect on new knowledge as a default.
• You are innovative and can add value to our team, you have good interpersonal skills, a collaborative attitude and ability to impact the support to marketed products.
• You have a high degree of flexibility as the tasks are varied, and the priority of projects and tasks may change.
• You are good at keeping an overview of your tasks and you are analytical and systematic and have excellent communication skills.
• It is an advantage if you have knowledge of secondary packaging.
• Your language proficiency in both written and spoken English is at a professional level.
About the department
You will join a team of dedicated and highly competent colleagues and be at the crossroad between Devices & Delivery Solutions (R&D), Quality, and Production. The department is supporting the entire range of Novo Nordisk products, and the technical product knowledge is anchored here. The team is responsible for the secondary packaging of the marketed products, and we own the specifications and material requirements.
We support numerous projects related to the above areas, as well as within SOP compliance, standardisations, training, technical customer compliant investigations and follow-up on quality activities.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Driving Change
At Novo Nordisk, we do not wait for change. We drive it. We are 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 are all working to move the needle on patient care.
Contact
For further information you can contact Senior Manager Søren Rønsted at +45 30775695.
Deadline
December 20th 2022
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified.
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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The position
In the role of Design Control & Quality Associate in Secondary Pack Maintenance you will function as a supporting element with own portfolio of tasks and responsibilities for assessing severity of identified risk and define requirements for our production lines to ensure patient safety and product quality. Further, you will be part of the product responsible team who ensures proper transfer of new developed products from our R&D division to the marketed portfolio of Device Manufacturing Development (DMD).
In Device Manufacturing Development (DMD), Secondary Pack Maintenance we own and maintain specifications for Novo Nordisk secondary packaging.
You can look forward to a position where your work has a high impact on the packaging of the products that reach the patients. The job will give you a great opportunity for working with innovative products on an international level and for having a broad range of contacts including production sites globally, sourcing & supply chain, R&D, Quality Assurance, regulatory affairs, customer service and affiliates.
Qualifications
• You might recently have graduated but you hold minimum a bachelor’s degree within engineering, natural sciences, or similar.
• Experience from working in or with a highly regulated industry, e.g. medico or pharmaceuticals, automotive or aerospace is a plus but not a prerequisite.
• You are very attentive to details and have a natural understanding of procedures and why these are important in a regulated industry.
• You are eager to learn and you reflect on new knowledge as a default.
• You are innovative and can add value to our team, you have good interpersonal skills, a collaborative attitude and ability to impact the support to marketed products.
• You have a high degree of flexibility as the tasks are varied, and the priority of projects and tasks may change.
• You are good at keeping an overview of your tasks and you are analytical and systematic and have excellent communication skills.
• It is an advantage if you have knowledge of secondary packaging.
• Your language proficiency in both written and spoken English is at a professional level.
About the department
You will join a team of dedicated and highly competent colleagues and be at the crossroad between Devices & Delivery Solutions (R&D), Quality, and Production. The department is supporting the entire range of Novo Nordisk products, and the technical product knowledge is anchored here. The team is responsible for the secondary packaging of the marketed products, and we own the specifications and material requirements.
We support numerous projects related to the above areas, as well as within SOP compliance, standardisations, training, technical customer compliant investigations and follow-up on quality activities.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Driving Change
At Novo Nordisk, we do not wait for change. We drive it. We are 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 are all working to move the needle on patient care.
Contact
For further information you can contact Senior Manager Søren Rønsted at +45 30775695.
Deadline
December 20th 2022
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified.
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.
Print job Send to e-mail
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 2.12.2022, 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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