Senior QA role within Global Contract Manufacturing
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Søborg
Are you looking for a place to feed your enthusiasm for quality? Are you passionate about ensuring the highest standards in quality processes? At Novo Nordisk, our team plays a vital role in overseeing the quality of Active Pharmaceutical Ingredients (APIs) and Drug Substances (DS) across our global network of Contract Manufacturing Organizations (CMOs). As part of the QA department, you'll collaborate with both internal and external partners, tackling complex challenges and making independent decisions that drive success. If you're ready to take on a leading role where your expertise can make a real difference every day, we want to hear from you! Join us and help shape the future of quality in one of the world's leading pharmaceutical companies. The position
In this position you will be responsible for Quality Assurance of Contract Manufacturing and will be responsible for one or more CMO´s with various products being produced for Novo Nordisk. The QA role includes: The quality responsibility for ensuring that our products are manufactured according to cGMP and our Marketing Authorizations. Numerous encounters daily with both internal and external business partners and a high level of complexity in your daily tasks. You should also contribute to continuous improvements of our processes and strive for simplicity without compromising quality. Handling of documentation from the contract manufacturers is a part of the job and you are also expected to participate in audits performed at the CMO and ensure sufficient follow up on CAPAs. QA support and GMP guidance to our partners and final release of the API and intermediates from CMO`s to the further process in Novo Nordisk. Expected travel is around 15-20 days a year as the Contract Manufacturing Organizations (CMOs) are located outside Denmark primarily Europe and US. If you are looking for a job which can foster the development of your professional and personal competences, this is your opportunity. Qualifications We are looking for an individual who can take ownership, work independently and make decisions that balance quality, expectations and business needs. To be successful in this role, you should have a degree in Pharmacy, Engineering or similar and have at least 4 years of experience in the pharmaceutical industry in manufacturing or quality control, where you have gained a solid and up-to-date knowledge of quality and GMP requirements. We look for a candidate who: Has a natural ability to take lead and work as a team player, and proactively contributes to the team’s tasks and activities. Has the ability to work in an international set-up with external stakeholders with different interests and agendas. Meets own deadlines and knows how to prioritize between different tasks in an ever-changing environment. Has great communication and collaboration skills and speaks and writes Danish and English fluently. About The Department
The GCM Drug Substance QA area is responsible for quality assurance and quality support to outsourced production activities worldwide. GCM DS QA is a dynamic area consisting of around 45 competent people with focus on either operations or projects. The department is characterized by a high level of professionalism, flexibility, and cooperation. The primary role of our area is to deliver QA support and set direction for our global CMOs. We focus on good social relations and prioritize to make room for fun at work. We have a great team spirit, and it is important for us that you will be a part of it.
At the moment, the workplace is in Søborg, but at the end of 2024 we will be relocated to Høje Taastrup. 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 Lena Ellen Larsen at +45 30756471 or at [email protected] Deadline
3 October 2024 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 this position you will be responsible for Quality Assurance of Contract Manufacturing and will be responsible for one or more CMO´s with various products being produced for Novo Nordisk. The QA role includes:
The GCM Drug Substance QA area is responsible for quality assurance and quality support to outsourced production activities worldwide. GCM DS QA is a dynamic area consisting of around 45 competent people with focus on either operations or projects. The department is characterized by a high level of professionalism, flexibility, and cooperation. The primary role of our area is to deliver QA support and set direction for our global CMOs. We focus on good social relations and prioritize to make room for fun at work. We have a great team spirit, and it is important for us that you will be a part of it.
At the moment, the workplace is in Søborg, but at the end of 2024 we will be relocated to Høje Taastrup. 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 Lena Ellen Larsen at +45 30756471 or at [email protected] Deadline
3 October 2024 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 Søborg.
Jobbet er oprettet på vores service den 12.9.2024, 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.
- Øvrige
- Søborg
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