QA Professional - Assembly and Pack in Global Contract Manufacturing
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Søborg
Would you like to work in one of the most interesting, complex and dynamic areas in Novo Nordisk? Global Contract Manufacturing (GCM) QA is responsible for quality assurance and quality support for outsourced production activities worldwide. Are you ready to engage, support and mobilise colleagues in an international business environment, where we both have business partners internal and external with CMO’s? Then you could be our new colleague in GCM QA, Søborg. The position
As QA Professional you will be responsible for quality assurance of contract manufacturing for assembly and pack CMOs. You will have to offer QA support and GMP guidance to our partners and do the final release of packaging from CMOs. Also, you will be responsible for ensuring that our products are manufactured according to cGMP and our marketing authorisations.
You will have numerous encounters daily with both internal and external business partners 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 5-15 days a year.
Qualifications To succeed in this role
You hold an MSc as Pharmacist, Engineer or similar. You have at least +2 years of experience from a pharmaceutical organisation where you have gained a solid and up-to-date knowledge of quality and GMP requirements. The ideal candidate is Qualified Person (QP) delegate and/or has knowledge of quality assurance of pharmaceutical manufactured products within assembly and pack and/or experience from working as QA for CMO’s. With your good cooperation and communication skills you are able to organise and drive tasks. You have a pragmatic approach to problem solving and strong interpersonal skills. You are detail-oriented with a strong quality mind set and are a team player but are also able to work independently. You thrive on working across departments in an international organisation. Great communication skills are a must, and you are expected to be fluent in English.
We are looking for an open-minded person with an outgoing attitude and natural networking skills. Additionally, we would enjoy welcoming a straightforward person with a good sense of humour to our department.
About the department
GCM QA is a dynamic department consisting of 50 competent people and is characterised by a high level of professionalism, flexibility and cooperation. The primary role of our department is to deliver QA support and set direction for our Global Contract Manufacturer Organisations worldwide. The open position as experienced QA is in the GCM QA Operations FP team, which is responsible for tablets, assembly and packaging at the CMO´s. Working at Novo Nordisk
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.
Contact
For further information, please contact Katrine Hammer on +45 3079 6624.
Deadline Please apply before December 10th, 2023. Interviews will be conducted on an ongoing basis.
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.
As QA Professional you will be responsible for quality assurance of contract manufacturing for assembly and pack CMOs. You will have to offer QA support and GMP guidance to our partners and do the final release of packaging from CMOs. Also, you will be responsible for ensuring that our products are manufactured according to cGMP and our marketing authorisations.
You will have numerous encounters daily with both internal and external business partners 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 5-15 days a year.
Qualifications To succeed in this role
We are looking for an open-minded person with an outgoing attitude and natural networking skills. Additionally, we would enjoy welcoming a straightforward person with a good sense of humour to our department.
About the department
GCM QA is a dynamic department consisting of 50 competent people and is characterised by a high level of professionalism, flexibility and cooperation. The primary role of our department is to deliver QA support and set direction for our Global Contract Manufacturer Organisations worldwide. The open position as experienced QA is in the GCM QA Operations FP team, which is responsible for tablets, assembly and packaging at the CMO´s. Working at Novo Nordisk
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.
Contact
For further information, please contact Katrine Hammer on +45 3079 6624.
Deadline Please apply before December 10th, 2023. Interviews will be conducted on an ongoing basis.
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 27.11.2023, 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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