Equipment Responsible
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Do you want to be part of shaping the innovative journey in Oral Finished Product - Quality Control (OFP QC)? Are you motivated by working with equipment within the laboratory field and ensuring it is handled the compliant way? If so, read more below and apply to become our new Equipment Responsible! 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 to maintain or qualify:
• laboratory equipment
• PAT
• new robotic solutions
• new automation projects in a laboratory setting
We are looking into two different positions – one as equipment responsible and one as qualification responsible - that will join us in an exciting time of expansion as we are working towards establishing a new laboratory that will be running by late summer.
You will take responsibility of already uprunning laboratory equipment e.g. UPLC/HPLC-, dissolution equipment and other laboratory equipment such as weights, UV, FTIR, Karl Fisher etc., or you will be helping to bring our new laboratory standards (e.g., automation and PAT equipment) to a GMP level of readiness 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 and 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 then share with your colleagues. You are team player but still enjoy to work 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 that 3-4 days are 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.
You will be joining Analytical Technology & Innovation, a newly established department, with the primary focus can be divided into the following areas:
1. Daily operations maintaining the full responsibility of all equipment in OFP QC
2. Implement new technology and complex equipment and automate existing laboratory processes
3. Find new innovative solutions for the laboratories.
We are currently looking for 2 positions within bullet 1 and 2 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 Anne Dorthe Vad Dockir +4530757037 Deadline
12 March 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 to maintain or qualify:
• laboratory equipment
• PAT
• new robotic solutions
• new automation projects in a laboratory setting
We are looking into two different positions – one as equipment responsible and one as qualification responsible - that will join us in an exciting time of expansion as we are working towards establishing a new laboratory that will be running by late summer.
You will take responsibility of already uprunning laboratory equipment e.g. UPLC/HPLC-, dissolution equipment and other laboratory equipment such as weights, UV, FTIR, Karl Fisher etc., or you will be helping to bring our new laboratory standards (e.g., automation and PAT equipment) to a GMP level of readiness 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 and 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 then share with your colleagues. You are team player but still enjoy to work 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 that 3-4 days are 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.
You will be joining Analytical Technology & Innovation, a newly established department, with the primary focus can be divided into the following areas:
1. Daily operations maintaining the full responsibility of all equipment in OFP QC
2. Implement new technology and complex equipment and automate existing laboratory processes
3. Find new innovative solutions for the laboratories.
We are currently looking for 2 positions within bullet 1 and 2 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 Anne Dorthe Vad Dockir +4530757037 Deadline
12 March 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 24.2.2023, 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.
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