Senior QA Professional - Medical Devices
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Hillerød
Do you want to play a vital part in the delivery of Novo Nordisk’s high-quality products to our patients? Are you an ambitious and proactive team player who sees collaboration as key to success? Then you might be the colleague we are missing in the quality assurance department of Device Manufacturing & Sourcing (DMS QA), read more and apply now!
The Position
You will be joining a great team of experienced and engaged QA professionals within DMS QA, and the focus will be on working with cloud-based data. As our new colleague you will be involved in many different responsibilities, but the following are some relevant pointers as to what the position entails: • Develop, maintain, and utilize data to proactively detect drifts in quality and improve the digitalisation of DMS QA
• Be responsible for digital projects in DMS QA or Contract Manufacturing & Sourcing, Devices & Sustainability if requested
• Be the QA responsible for release of components produced from our internal production
• Support to deviation handling as well as change requests for the area
• Always having a focus on continuous improvements and simplification of our processes We also welcome applicants from other branches, as long as you share our passion for quality, GMP and problem-solving and are keen to acquire professional competencies to become what we describe as an “ideal candidate”. Also, if you are in the fall of your professional career and would enjoy requiring new competencies you are also welcomed to apply. We are part of the Novo Nordisk Quality organisation where we enforce compliance on behalf of authorities, support the business and at the same time strive towards making daily work for ourselves and our stakeholders less complex. Qualifications We are looking for someone who is curious and seek to understand the underlying complexities and gain energy by going on the shopfloor and interact with stakeholders or through dialog within their team. To succeed in this role, you: • Have a bachelor's or master's degree in Software Engineering, Data Engineering, Robotics, Data Science or similar
• Have several years of experience in a QA role in a pharmaceutical company
• Are familiar with most of the following technologies: SQL, Python, Linux, CI/CD, AWS (or other cloud solutions) as well as DevOps
• Are fluent in both English and Danish Knowledge of ISO13485, GMP, validation and Lean will be seen an advantage, as well as previous experience in the medical devices area. As a person, you bring a positive mindset, you are good at establishing relations with other people, communicate constructively, and you have a systematic approach to problem-solving. You are proactive and have a great interest in developing yourself and the team you are a part of.
About the department
DMS QA consists of 19 highly qualified colleagues and is responsible for QA of the in-house production as well as the global supply chain of high-quality components and preassembled parts for all Novo Nordisk prefilled and durable devices. Our external suppliers are in Europe, China, USA and Brazil. Our main purpose is to safeguard patient safety, product quality and compliance.
We work in lovely surroundings in Novo Nordisk Device Manufacturing and Sourcing's buildings in Hillerød about 30 km north of Copenhagen. Contacts
If you want to know more about the position, please contact Associate Manager Paw Winther Brandt-Kofoed by phone on +45 34 48 00 98. Please note that Paw is currently out of office and will be available to be contacted from October the 30th.
Deadline
14 November 2023 You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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 Position
You will be joining a great team of experienced and engaged QA professionals within DMS QA, and the focus will be on working with cloud-based data. As our new colleague you will be involved in many different responsibilities, but the following are some relevant pointers as to what the position entails: • Develop, maintain, and utilize data to proactively detect drifts in quality and improve the digitalisation of DMS QA
• Be responsible for digital projects in DMS QA or Contract Manufacturing & Sourcing, Devices & Sustainability if requested
• Be the QA responsible for release of components produced from our internal production
• Support to deviation handling as well as change requests for the area
• Always having a focus on continuous improvements and simplification of our processes We also welcome applicants from other branches, as long as you share our passion for quality, GMP and problem-solving and are keen to acquire professional competencies to become what we describe as an “ideal candidate”. Also, if you are in the fall of your professional career and would enjoy requiring new competencies you are also welcomed to apply. We are part of the Novo Nordisk Quality organisation where we enforce compliance on behalf of authorities, support the business and at the same time strive towards making daily work for ourselves and our stakeholders less complex. Qualifications We are looking for someone who is curious and seek to understand the underlying complexities and gain energy by going on the shopfloor and interact with stakeholders or through dialog within their team. To succeed in this role, you: • Have a bachelor's or master's degree in Software Engineering, Data Engineering, Robotics, Data Science or similar
• Have several years of experience in a QA role in a pharmaceutical company
• Are familiar with most of the following technologies: SQL, Python, Linux, CI/CD, AWS (or other cloud solutions) as well as DevOps
• Are fluent in both English and Danish Knowledge of ISO13485, GMP, validation and Lean will be seen an advantage, as well as previous experience in the medical devices area. As a person, you bring a positive mindset, you are good at establishing relations with other people, communicate constructively, and you have a systematic approach to problem-solving. You are proactive and have a great interest in developing yourself and the team you are a part of.
About the department
DMS QA consists of 19 highly qualified colleagues and is responsible for QA of the in-house production as well as the global supply chain of high-quality components and preassembled parts for all Novo Nordisk prefilled and durable devices. Our external suppliers are in Europe, China, USA and Brazil. Our main purpose is to safeguard patient safety, product quality and compliance.
We work in lovely surroundings in Novo Nordisk Device Manufacturing and Sourcing's buildings in Hillerød about 30 km north of Copenhagen. Contacts
If you want to know more about the position, please contact Associate Manager Paw Winther Brandt-Kofoed by phone on +45 34 48 00 98. Please note that Paw is currently out of office and will be available to be contacted from October the 30th.
Deadline
14 November 2023 You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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.
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 11.10.2023, 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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