Advanced QA Professional - Small Molecules API
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Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in ensuring the quality and safety of products for clinical trials and be part of an exciting growth journey within our small molecules’ portfolio? If so, we have an exciting possibility waiting for you as Advanced QA Professional in Chemistry, Manufacturing and Control (CMC) Active Pharmaceutical Ingredients (API) QA, read more and apply now! The position Novo Nordisk is expanding within chemically synthesized APIs (small molecules API) and in this position, you will be working with API release for clinical trials from Contract Manufacturing Organisations (CMO). In your daily work you will challenge and approve documents related to development, manufacture, stability, and release of clinical batches. In addition, you will be a part of our product development projects ensuring that our products can be used in clinical trials worldwide.
We do value flexibility, and we offer a hybrid working model, but due to the nature of the role you will be working on site at least 3 days per week. Qualifications The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural urge to handle quality issues at the right level, make decisions and follow-up on quality related problems. To succeed in this role, you: hold a university Bachelor or Master in Pharmacy, Engineering, Biology, Chemistry or similar. have experience in a pharmaceutical company, ideally also within small molecules and/or in a QA role. have a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production. are proficient in English. If you have been working in QA and/or with small molecules, APIs and/or CMOs, it will be seen as an advantage. On a personal level, you are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks. You thrive in a dynamic environment, where teamwork is on top of the agenda, and you like working with many different stakeholders – internally and externally.
About the department You will become part of a growing CMC API department consisting of two teams where we today are 30 dedicated colleagues. We are currently building up competencies within API small molecules and therefore you will be reporting directly to the QA Director. Our department culture ensures a healthy and fun working environment where we value strong relationships, people growth and optimisation of our processes. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release API for clinical trials. As part of Novo Nordisk Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients. 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 QA Director Rikke Wissing Jensen +45 3075 1566 Deadline
21. january 2024 Please note that interviews will be scheduled as soon as relevant candidates are identified, so we encourage you to apply sooner rather than later. 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.
We do value flexibility, and we offer a hybrid working model, but due to the nature of the role you will be working on site at least 3 days per week. Qualifications The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural urge to handle quality issues at the right level, make decisions and follow-up on quality related problems. To succeed in this role, you:
About the department You will become part of a growing CMC API department consisting of two teams where we today are 30 dedicated colleagues. We are currently building up competencies within API small molecules and therefore you will be reporting directly to the QA Director. Our department culture ensures a healthy and fun working environment where we value strong relationships, people growth and optimisation of our processes. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release API for clinical trials. As part of Novo Nordisk Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients. 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 QA Director Rikke Wissing Jensen +45 3075 1566 Deadline
21. january 2024 Please note that interviews will be scheduled as soon as relevant candidates are identified, so we encourage you to apply sooner rather than later. 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.
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Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 3.1.2024, 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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