QA with proactive mindset and strong communication skills
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Måløv
Are you an experienced QA, with strong communication skills, who is eager to set direction and to ensure compliance, in close collaboration with colleagues and stakeholders? If so, we have a 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 and you will have the overview of the processes within production of oral medicinal products. In QA we have the quality oversight and are physically present in the production to observe performed processes and help solve issues in real time. To succeed in your role, you will proactively improve the processes, together with your colleagues and stakeholders, in order to ensure the right quality level and cLEAN processes.
You will perform review of batch documentation as well as review of batch and 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.
You will set directions and deliver results which have a significant impact within the context of our business. Your focus will be assuring that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements. You have a risk-based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
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
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 60 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.
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 Associate Manager Linea Frenk Alsing +45 3075 6596.
Deadline
Deadline to apply for this position is 19th of December 2022.
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.
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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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 and you will have the overview of the processes within production of oral medicinal products. In QA we have the quality oversight and are physically present in the production to observe performed processes and help solve issues in real time. To succeed in your role, you will proactively improve the processes, together with your colleagues and stakeholders, in order to ensure the right quality level and cLEAN processes.
You will perform review of batch documentation as well as review of batch and 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.
You will set directions and deliver results which have a significant impact within the context of our business. Your focus will be assuring that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements. You have a risk-based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
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 have 3+ years of experience with GMP, quality assurance or production support.
- You are an open-minded person with high level of energy, an outgoing attitude and have very strong communication and collaboration skills.
- You have an innovative mind and are able to see new and optimized solutions.
- 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 the top of the agenda, and like working with many different stakeholders.
- You have a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity.
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 60 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.
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 Associate Manager Linea Frenk Alsing +45 3075 6596.
Deadline
Deadline to apply for this position is 19th of December 2022.
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.
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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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 2.12.2022, 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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