Process Validation Responsible
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Måløv
Do you want to join some amazing colleagues with a clear purpose in a great working environment? Would you like to use your knowledge, and help us scaling up a production facility, which is constantly undergoing development? Are you ready to take responsibility and do you have a quality focus for ensuring operational tablet production in a manufacturing setup with very high-quality standards? If yes, then you could be our new Process Validation responsible. Apply today!
The position
We currently have an open position in our Project and implementation team, within the department OFP Bulk production. The purpose of the department is to produce oral products to market. In this position, you will be responsible for preparing, executing, and reporting process validation. Furthermore, you will be responsible for providing processes knowledge during scoping of different projects. You will work in close collaboration with project managers and area specialists within your team.
You will be responsible for carrying out daily tasks that include:
• Work as operational responsible and author process validation documents.
• Work with project managers to prepare and execute process validation.
• Provide input during the scope phase of various project activities, serving as a process subject matter expert (SME).
• Ensure that all project activities are timely completed and in compliance with Novo Nordisk quality system.
• Participate in activities in multi-disciplinary project groups, in which you work closely with experts from a wide range of areas. Qualifications
To be successful in the role we expect you:
• Hold a master’s degree and/or a PhD in science within Pharmacy, Chemistry, Engineering, or a similar field.
• Have demonstrated experience in authoring, executing, and reporting validation/qualification documents in a GMP manufacturing or process development (preferably within process validation).
• Have strong written and verbal communication skills to author clear and concise validation documents.
• If you have proficiency in data and statistical analysis it is a plus.
On a personal level you have a detail-oriented mindset and are quick to acquire new knowledge. You take pride in driving tasks forward and meeting deadlines. We also emphasize that you are a team-player who can motivate the people around you, and you are motivated to mentor and guide less experienced colleagues.
About the department
OFP is organizationally located in Product Supply, which globally employs approx. 14,000 of Novo Nordisk more than 43,000 employees. In OFP, we are steadily growing and at present we are approximately 1100 committed colleagues in Måløv. We have great ambitions for the future, and we are working hard to get our new product successfully distributed to the market. About Oral Finished Products
In 2004 Novo Nordisk initiated the ambitious and pioneering work of being the first company to offer a GLP-1 based oral alternative, to type2 diabetes patients all over the world. In 2019 we got the first approval to send our GLP-1 based tablet to the market, and we are already represented in both US, EU and other parts of the world. The pioneer spirit is what characterise Oral Finished Products. Every day we put our very best efforts in optimising and developing our production, to be able to help even more patients all over the world. And to succeed with that we need you! So get on board, our fantastic journey has just begun.
Contact
For further information, you are welcome to contact Associate Manager Henrik Vestergaard Frandsen, +45 3079 1808
Deadline
12 November, 2023 but we review applications on an ongoing basis, so do not hesitate to apply as soon as possible. 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
We currently have an open position in our Project and implementation team, within the department OFP Bulk production. The purpose of the department is to produce oral products to market. In this position, you will be responsible for preparing, executing, and reporting process validation. Furthermore, you will be responsible for providing processes knowledge during scoping of different projects. You will work in close collaboration with project managers and area specialists within your team.
You will be responsible for carrying out daily tasks that include:
• Work as operational responsible and author process validation documents.
• Work with project managers to prepare and execute process validation.
• Provide input during the scope phase of various project activities, serving as a process subject matter expert (SME).
• Ensure that all project activities are timely completed and in compliance with Novo Nordisk quality system.
• Participate in activities in multi-disciplinary project groups, in which you work closely with experts from a wide range of areas. Qualifications
To be successful in the role we expect you:
• Hold a master’s degree and/or a PhD in science within Pharmacy, Chemistry, Engineering, or a similar field.
• Have demonstrated experience in authoring, executing, and reporting validation/qualification documents in a GMP manufacturing or process development (preferably within process validation).
• Have strong written and verbal communication skills to author clear and concise validation documents.
• If you have proficiency in data and statistical analysis it is a plus.
On a personal level you have a detail-oriented mindset and are quick to acquire new knowledge. You take pride in driving tasks forward and meeting deadlines. We also emphasize that you are a team-player who can motivate the people around you, and you are motivated to mentor and guide less experienced colleagues.
About the department
OFP is organizationally located in Product Supply, which globally employs approx. 14,000 of Novo Nordisk more than 43,000 employees. In OFP, we are steadily growing and at present we are approximately 1100 committed colleagues in Måløv. We have great ambitions for the future, and we are working hard to get our new product successfully distributed to the market. About Oral Finished Products
In 2004 Novo Nordisk initiated the ambitious and pioneering work of being the first company to offer a GLP-1 based oral alternative, to type2 diabetes patients all over the world. In 2019 we got the first approval to send our GLP-1 based tablet to the market, and we are already represented in both US, EU and other parts of the world. The pioneer spirit is what characterise Oral Finished Products. Every day we put our very best efforts in optimising and developing our production, to be able to help even more patients all over the world. And to succeed with that we need you! So get on board, our fantastic journey has just begun.
Contact
For further information, you are welcome to contact Associate Manager Henrik Vestergaard Frandsen, +45 3079 1808
Deadline
12 November, 2023 but we review applications on an ongoing basis, so do not hesitate to apply as soon as possible. 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 18.10.2023, 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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