Advanced Quality Assurance Professional
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Hillerød
Are you seeking exciting new development opportunities? Do you find Quality Systems and validation intriguing? Do you believe in Novo Nordisk values? Do you have a passion for Good Manufacturing Practice? and would you like to safeguard our patients? Then I may have just the right job for you in Device Manufacturing Development (DMD) Quality Assurance (QA) team.
The role is anchored in Hillerød, Denmark, but you will have stakeholders across the globe. The position You will be joining a great team of experienced and engaged QA professionals within Device Manufacturing Development (DMD). Our key responsibility is the development of new devices, as well as new assembly and packaging lines, and we support Pilot Operations in the validation of production lines and production of clinical trials among many other contact interfaces. As our new QA you will be involved in many different responsibilities for example: QA ensuring compliance within our Quality Management System, QA for the Packaging process including QA oversight in the production facility and QA for our Logistics and Warehouse processes. You will set direction for quality and compliance, based on the ever-increasing demands of the authorities and always having a focus on continuous improvements and simplification of our processes. As DMD is a test facility, you can handle complex tasks and adapt to a volatile environment, and you thrive in a work life where every day brings something different Finally, it is important that you are open-minded and have good communication and collaboration skills. In this role, you will encounter many colleagues across and beyond a diverse organisation. You will quickly come to understand that alternative ways of thinking, different cultural/educational backgrounds, and variety of age and experience, are key elements to our success. We strongly believe in a very thorough on-boarding, that will bring you closer to be a success in the role. Besides that, we encourage all our employee to take responsibility, together with us, for their professional and personal development. Qualifications To be successful in this role, we envision you as someone who: Holds a master’s degree in Pharmacy, engineering, or other relevant area. Experience with GMP related to the pharmaceutical industry, preferable within manufacturing or QA Can communicate at a proficient level in both oral and written English. Is well-structured in his/her approach to tasks, thorough and efficient in execution of responsibilities Is a team-player at heart and enjoys interacting, as well as guiding others in an inclusive and trusting manner Experience with validation activities will be an advantage. About the department In Device Manufacturing Development Quality Assurance, we are 25 highly engaged colleagues. We are responsible for assuring quality and compliance of all processes in DMD. This includes product maintenance, design control, testing, manufacturing development and manufacturing processes ranging from developing and transferring components for new devices for our patients with diabetes and rare deceases, to process ownership of packaging materials, assembly, and packaging lines to product maintenance of devices. We are constantly improving our competences and our way of working by focusing on simplicity, agility, and collaboration for us to be able to deliver the best possible support to the business. The team is a diverse team and thrive with the great variety of tasks, and we value and prioritize teamwork with a high degree of individual accountability and flexibility. You will be a part of a team which consist of 25 dedicated colleagues, a team who takes care of each other and support each other. As an employee in the team, you will be able to take up a lot of responsibility and gain support to develop. You can expect to grow both on a personal and professional level. You will see me and experience me as leader, with a positive and agile mindset, to embrace change and adjustment to improve processes and quality for the future demands. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact For clarifications or questions, please contact Mikkel Mølvig Dalsø (+45 30 77 50 01) Deadline March 5th, 2023. I will look at applications and perform interviews continuously - and hire if the perfect match is found prior to this deadline. It might be you. We are eager to welcome our new colleague. 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.
The role is anchored in Hillerød, Denmark, but you will have stakeholders across the globe. The position You will be joining a great team of experienced and engaged QA professionals within Device Manufacturing Development (DMD). Our key responsibility is the development of new devices, as well as new assembly and packaging lines, and we support Pilot Operations in the validation of production lines and production of clinical trials among many other contact interfaces. As our new QA you will be involved in many different responsibilities for example: QA ensuring compliance within our Quality Management System, QA for the Packaging process including QA oversight in the production facility and QA for our Logistics and Warehouse processes. You will set direction for quality and compliance, based on the ever-increasing demands of the authorities and always having a focus on continuous improvements and simplification of our processes. As DMD is a test facility, you can handle complex tasks and adapt to a volatile environment, and you thrive in a work life where every day brings something different Finally, it is important that you are open-minded and have good communication and collaboration skills. In this role, you will encounter many colleagues across and beyond a diverse organisation. You will quickly come to understand that alternative ways of thinking, different cultural/educational backgrounds, and variety of age and experience, are key elements to our success. We strongly believe in a very thorough on-boarding, that will bring you closer to be a success in the role. Besides that, we encourage all our employee to take responsibility, together with us, for their professional and personal development. Qualifications To be successful in this role, we envision you as someone who:
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 14.2.2023, 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.
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- Hillerød
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Statistik over udbudte øvrige over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 2. maj 2024 | 69 |
| 1. maj 2024 | 73 |
| 30. april 2024 | 74 |
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