Senior QA Professional with passion for quality and contract manufacturing
Denne stilling er desværre ikke længere ledig.
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Søborg
Are you looking for an opportunity where you can release your passion for quality? Are you excited about playing a crucial role in ensuring quality processes in Novo Nordisk’s global network of Contract Manufacture Organizations (CMOs)? Most importantly, are you eager to contribute with your energy to a diverse team that works hard to bring benefits to our patients and stakeholders? Working in our team will give you both great professional and personal development opportunities in a well-functioning department. We can offer you a great working environment with a high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. The position
As a QA Professional you will be responsible for the quality assurance of contract manufacturing, and you will be responsible for one or more CMO`s. You will have to offer QA support and GMP guidance to our partners and do the final release of the API and intermediates from CMO`s to the further processes in Novo Nordisk Also, you will be responsible for ensuring that our products are manufactured according to cGMP and our authorisations.
You will have numerous encounters daily with both internal and external stakeholders and you should expect a high level of complexity in your daily tasks. You will solve a wide variety of tasks and have a great opportunity to be challenged every day. The daily QA activities are typically carried out by the contract manufacturers themselves, but the handling of documentation from the contract manufacturers is a part of the job. Since the manufacturers are located outside Denmark, you are expected to travel 15-20 days a year.
Qualifications
You hold an academic degree as Pharmacist, Engineer or similar You have at least 4 years of experience from a pharmaceutical organisation where you have gained a solid and up-to-date knowledge of quality and GMP requirements i.e. Non-Conformity (NC), Corrective Actions and Preventive Actions (CAPA) handling, change control, complaints, Annual Product Review (APR) and validations. The ideal candidate is a Qualified Person (QP) delegate and/or has thorough knowledge of quality assurance of pharmaceutical manufactured products. Good cooperation and communication skills that makes you excellent at organising and driving tasks. You have a pragmatic approach to problem solving and strong interpersonal skills. You are detail-oriented with a strong quality mindset and a team-player, but you are also able to work independently. You thrive working across departments in an international organisation. Great communication skills are mandatory, and you are expected to be fluent in Danish and English. About the department
GCM QA is a dynamic department that consists of 40 competent colleagues and is characterised by a high level of professionalism, flexibility, and cooperation. The primary role of our department is delivering QA support and set direction for our Global Contract Manufacturer Organisations worldwide. We focus on good social relations and well-being in the team and prioritise to make room for fun at work.
Contact
For further information, please contact Birgitte Madsen Find on +45 3075 4482.
Deadline 9th July Applications will be reviewed on an ongoing basis. 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.
As a QA Professional you will be responsible for the quality assurance of contract manufacturing, and you will be responsible for one or more CMO`s. You will have to offer QA support and GMP guidance to our partners and do the final release of the API and intermediates from CMO`s to the further processes in Novo Nordisk Also, you will be responsible for ensuring that our products are manufactured according to cGMP and our authorisations.
You will have numerous encounters daily with both internal and external stakeholders and you should expect a high level of complexity in your daily tasks. You will solve a wide variety of tasks and have a great opportunity to be challenged every day. The daily QA activities are typically carried out by the contract manufacturers themselves, but the handling of documentation from the contract manufacturers is a part of the job. Since the manufacturers are located outside Denmark, you are expected to travel 15-20 days a year.
Qualifications
GCM QA is a dynamic department that consists of 40 competent colleagues and is characterised by a high level of professionalism, flexibility, and cooperation. The primary role of our department is delivering QA support and set direction for our Global Contract Manufacturer Organisations worldwide. We focus on good social relations and well-being in the team and prioritise to make room for fun at work.
Contact
For further information, please contact Birgitte Madsen Find on +45 3075 4482.
Deadline 9th July Applications will be reviewed on an ongoing basis. 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 26.6.2023, 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
- Søborg
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