QA professional - 18 months temporary position
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Måløv
Are you passionate about working within Quality Assurance (QA) and eager to learn and have strong communication and collaboration skills. If so, we have a temporary position in a fast-growing tablet production in Måløv. You will be part of a team with responsibility for quality assurance for bulk and packaging production of tablets in Oral Finished Product QA. You will have influence and set directions in setting the right level of compliance, optimizing our processes in collaboration with stakeholders. We can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. In OFP QA our department consist of colleagues based in both Måløv and Durham US.
The Position
You will be part of the QA releasing team in OFP QA. Your main responsibility will be review of batch documentation and QA approval of several different types of documents and processes related to the daily operation for production and packaging of tablets in Oral Finished Product QA (OFP QA). Our core task is to ensure that we get products out to our patients at the right quality and in a timely manner. You will perform review of batch documentation, perform oversight in production and approve process related documentation from our stakeholders including deviations, change requests, SOPs etc. Our core task is to ensure that we get products out to our patients at the right quality and in a timely manner. The temporary position for 18 months is from 1st of April 2023 to 31th of September 2024. We can offer an exciting and challenging position, where you become part of a competent team that acts as sparring partners and problem solvers in quality issues for the production.
Qualifications
• You hold a MSc in Pharmacy, Microbiology, Veterinary medicine or similar
• You are newly graduated or have a couple of years of experience
• You are an open-minded person with high level of energy, an outgoing attitude and have strong communication and collaboration skills
• You thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders
As we operate both in a national and an international environment, you must speak and write Danish and English fluently.
About the department
Oral Finished Products QA is a department which employ approximately 70 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.
Contact
For further information, please contact Associate Manager Linea Frenk Alsing +45 3075 6596. Deadline
Deadline to apply for this position is February 23th 2023. Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline. 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.
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.
The Position
You will be part of the QA releasing team in OFP QA. Your main responsibility will be review of batch documentation and QA approval of several different types of documents and processes related to the daily operation for production and packaging of tablets in Oral Finished Product QA (OFP QA). Our core task is to ensure that we get products out to our patients at the right quality and in a timely manner. You will perform review of batch documentation, perform oversight in production and approve process related documentation from our stakeholders including deviations, change requests, SOPs etc. Our core task is to ensure that we get products out to our patients at the right quality and in a timely manner. The temporary position for 18 months is from 1st of April 2023 to 31th of September 2024. We can offer an exciting and challenging position, where you become part of a competent team that acts as sparring partners and problem solvers in quality issues for the production.
Qualifications
• You hold a MSc in Pharmacy, Microbiology, Veterinary medicine or similar
• You are newly graduated or have a couple of years of experience
• You are an open-minded person with high level of energy, an outgoing attitude and have strong communication and collaboration skills
• You thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders
As we operate both in a national and an international environment, you must speak and write Danish and English fluently.
About the department
Oral Finished Products QA is a department which employ approximately 70 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.
Contact
For further information, please contact Associate Manager Linea Frenk Alsing +45 3075 6596. Deadline
Deadline to apply for this position is February 23th 2023. Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline. 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.
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 Måløv.
Jobbet er oprettet på vores service den 3.2.2023, 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
- Måløv
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