QA Specialist
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Gentofte
Are you ready to play a crucial role in shaping the future of life-changing products for patients battling chronic diseases? Do you love working closely with talented colleagues and experts in your field? Want to join a skilled team at the forefront of new products and digital innovation? If yes, then you might be the right fit to join our colleagues in BRD (Biotech & Rare diseases) API (Active Pharmaceutical Ingredients) QA. Read more and apply! The position
In QA, our main goal is to guarantee top-quality products for our patients. With various new products and technologies emerging in BRD, we're looking for more expertise in Process/Facility/Validation to strengthen our team. Your main responsibilities will include:
• Working together with the management team to set the future strategy
• Supporting implementation of our ambitious goals
• Finding automated solutions that seamlessly blend quality and compliance while optimizing production
• Cooperating with production and QA colleagues We believe that LEAN, GMP and digitalisation supports one another in the best way! Qualifications
We are looking for someone who can take charge, work independently, and make decisions that balance quality, expectations, and business needs.
To succeed in this role, you:
• Hold a master’s degree within a relevant field e.g. Engineering, Pharmacy, or similar
• Have extensive experience in a QA role
• Have proven experience with GMP manufacturing in the pharmaceutical industry
• Have good stakeholder management skills and collaboration skills at all levels of the organization
• Are fluent in English both written and spoken
Moreover, we are looking for an individual that is flexible and have a strong quality mind-set combined with the ability to simplify processes.
We appreciate a curious, innovative, and solution-oriented approach to overcome challenges. We expect you to value good workplace relationships and contribute positively to a good working environment, also communicating clearly in a good tone. About the department
As a Quality Assurance Specialist, you will be referring directly to the Quality Director, and you will join a department of highly skilled and experienced colleagues. The teams have a high level of self-governance, and the working relations are informal. We value good humour and an open and honest culture. We appreciate a colleague who takes responsibility, has a positive and curious approach to drive new challenges and contributes to a pleasant working atmosphere. We have a high focus on a great work-life balance, with the flexibility to work from the office and remote. We are more than 60 employees in the department covering the production of API in BRD DK across our sites in Hillerød, Kalundborg and Gentofte. You will be part of the management team, consisting of the department head, department assistant, 5 associate managers and 3 other specialists.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for 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
For further information, please contact Director Jane Karina Nielsen on +45 3079 8795 Deadline
12 November 2023 Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. 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.
In QA, our main goal is to guarantee top-quality products for our patients. With various new products and technologies emerging in BRD, we're looking for more expertise in Process/Facility/Validation to strengthen our team. Your main responsibilities will include:
• Working together with the management team to set the future strategy
• Supporting implementation of our ambitious goals
• Finding automated solutions that seamlessly blend quality and compliance while optimizing production
• Cooperating with production and QA colleagues We believe that LEAN, GMP and digitalisation supports one another in the best way! Qualifications
We are looking for someone who can take charge, work independently, and make decisions that balance quality, expectations, and business needs.
To succeed in this role, you:
• Hold a master’s degree within a relevant field e.g. Engineering, Pharmacy, or similar
• Have extensive experience in a QA role
• Have proven experience with GMP manufacturing in the pharmaceutical industry
• Have good stakeholder management skills and collaboration skills at all levels of the organization
• Are fluent in English both written and spoken
Moreover, we are looking for an individual that is flexible and have a strong quality mind-set combined with the ability to simplify processes.
We appreciate a curious, innovative, and solution-oriented approach to overcome challenges. We expect you to value good workplace relationships and contribute positively to a good working environment, also communicating clearly in a good tone. About the department
As a Quality Assurance Specialist, you will be referring directly to the Quality Director, and you will join a department of highly skilled and experienced colleagues. The teams have a high level of self-governance, and the working relations are informal. We value good humour and an open and honest culture. We appreciate a colleague who takes responsibility, has a positive and curious approach to drive new challenges and contributes to a pleasant working atmosphere. We have a high focus on a great work-life balance, with the flexibility to work from the office and remote. We are more than 60 employees in the department covering the production of API in BRD DK across our sites in Hillerød, Kalundborg and Gentofte. You will be part of the management team, consisting of the department head, department assistant, 5 associate managers and 3 other specialists.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for 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
For further information, please contact Director Jane Karina Nielsen on +45 3079 8795 Deadline
12 November 2023 Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. 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 Gentofte.
Jobbet er oprettet på vores service den 24.10.2023, 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.
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Statistik over udbudte jobs som øvrige i Gentofte
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Statistik over udbudte øvrige i Gentofte over tid
Dato | Alle jobs som øvrige |
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4. november 2024 | 19 |
3. november 2024 | 19 |
2. november 2024 | 19 |
1. november 2024 | 19 |
31. oktober 2024 | 17 |
30. oktober 2024 | 16 |
29. oktober 2024 | 16 |
28. oktober 2024 | 16 |
27. oktober 2024 | 18 |
26. oktober 2024 | 18 |
25. oktober 2024 | 16 |
24. oktober 2024 | 19 |
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5. oktober 2024 | 23 |