Qualification Professional for QC
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Would you love to be part of shaping the innovative journey in Oral Finished Product - Quality Control (OFP QC)? Are you motivated by working with new equipment within the laboratory field and ensuring it is qualified to production? If so, read more below and apply to become our new qualification employee! The position
As Equipment Responsible within OFP QC, you will be working in a cross-disciplinary team, handling of a broad spectrum of tasks within laboratory equipment, automation, and Process Analytical Technology (PAT). The main task will be qualification and working in projects with new equipment, such as. laboratory equipment PAT new robotic solutions new automation projects in a laboratory setting You will be responsible for qualification of new equipment and already running laboratory equipment e.g. UPLC/HPLC-, dissolution equipment and other laboratory equipment such as weights, UV, FTIR, Karl Fisher etc. Furthermore, you will work close together with the innovation team, on new equipment such as PAT, robotic solutions so we can get OFP QC up to QC 4.0 standard. Qualifications
We are looking for someone that has sufficient insight on laboratory equipment or other kind of production equipment within the pharmaceutical industry, who can lead documentation, compliance, qualification, maintenance and can facilitate verification and validation activities including test execution, documentation review and approval. Ideally, you have experience within laboratory equipment, or you have been responsible for similar equipment maintenance incl. troubleshooting, test and documentation. To succeed in this role, you: hold a bachelor’s degree in chemistry, pharmacy, engineering or similar have minimum 1 year of experience within the pharmaceutical industry are knowledgeable in GMP, especially regarding automation/robots’ projects have full proficiency in both Danish and English Furthermore, you have experience with some of the following: delivery of complete validation packages, Requirement specifications, Installation/Operational/Performance Qualification Protocol/Report, Operation and Maintenance SOPs.
On a personal level, you have a detail-oriented mindset and quickly acquire new knowledge that you will share with your colleagues. You are team player but still enjoy working independently. You have a sincere interest in laboratory equipment and exploring innovative technologies and you enjoy being part of a team where it is important to have fun and where we work in a collaborative and trusting atmosphere. The workplace is placed in Måløv, where the work language is Danish, and it is required to be 3-4 days on-site.
About the department
OFP is organisationally located in Product Supply, which globally employs approx. 2.000 of Novo Nordisk more than 43.000 employees. The OFP QC area consist of approx. 175 dedicated colleagues newly divided in 3 departments, Market Release, New Product Entry and Analytical technology and Innovation.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact
For further information, please contact Jimmie Slott Madsen 30795992 Deadline
14th Maj 2023 Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible. 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 Equipment Responsible within OFP QC, you will be working in a cross-disciplinary team, handling of a broad spectrum of tasks within laboratory equipment, automation, and Process Analytical Technology (PAT). The main task will be qualification and working in projects with new equipment, such as.
We are looking for someone that has sufficient insight on laboratory equipment or other kind of production equipment within the pharmaceutical industry, who can lead documentation, compliance, qualification, maintenance and can facilitate verification and validation activities including test execution, documentation review and approval. Ideally, you have experience within laboratory equipment, or you have been responsible for similar equipment maintenance incl. troubleshooting, test and documentation. To succeed in this role, you:
On a personal level, you have a detail-oriented mindset and quickly acquire new knowledge that you will share with your colleagues. You are team player but still enjoy working independently. You have a sincere interest in laboratory equipment and exploring innovative technologies and you enjoy being part of a team where it is important to have fun and where we work in a collaborative and trusting atmosphere. The workplace is placed in Måløv, where the work language is Danish, and it is required to be 3-4 days on-site.
About the department
OFP is organisationally located in Product Supply, which globally employs approx. 2.000 of Novo Nordisk more than 43.000 employees. The OFP QC area consist of approx. 175 dedicated colleagues newly divided in 3 departments, Market Release, New Product Entry and Analytical technology and Innovation.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact
For further information, please contact Jimmie Slott Madsen 30795992 Deadline
14th Maj 2023 Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible. 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 Måløv.
Jobbet er oprettet på vores service den 27.4.2023, 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.
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