Operational Responsible Formulation & Filtration
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Måløv
Are you motivated by working in a changing environment? Would you like to be involved in a new capacity expansion project, in which you can influence and impact future Aseptic Production (AP) production facilities? If yes, we offer a great opportunity to become part of a team, where we turn ideas into actions. Apply today, and become our new Operational Responsible for Formulation and Filtration. The Position
In Biotech & Rare Diseases (BRD) expansion project in Måløv, we are planning to expand our production facilities. The aim of this new expansion project is to build a completely new manufacturing facility, including the implementation of isolator and other advanced technologies, with which Novo Nordisk has limited experience. This new facility aims to innovate our processes and to broaden our perspective, which is why this position requires a candidate with a good innovative mindset.
As our Operational Responsible for Formulation and Filtration, your main area of responsibility is getting processes and procedures ready for production.
Therefore, your main tasks will be:
• Responsible for filling all formulation and filtration activities.
• Project management and execution, including integration and cooperation with the program mirror organisation.
• Ensure that Systematic Problem Solving (SPS) and process confirmation are carried out in a structured way, and implementation of LEAN methodologies in the work carried out.
• Responsible for Quality and Compliance, ensuring that internal and internal quality demands comply to Current Good Manufacturing Practice (CGMP).
Though the project is located in Målev, interaction with the AP Expansion project on other sites is needed, and some travel or online-activity across the world, and time zones must be expected.
Qualifications To be considered for this position you have:
• An academic degree (BSc., MSc. or PhD.)
• Solid understanding of Current Good Manufacturing Practice (GMP)
• Preferably 5 years of project management experience, and/or Formulation and Filtration.
• Solid network within Product Supply (PS) and related areas within Novo Nordisk, or a lot of experience within the pharmaceutical industry.
• High verbal and written communication skills in English, plus good presentation skills. As a person, you have good cooperation and communications skills, and you are able to engage and coach own subordinates and other project team members. You are comfortable with working in an environment in constant change, with high complexity, and you are able to optimize, create and implement new working practices. You are result-oriented with a “can-do” attitude, being structured and organized with strong focus on high quality. About the Department Our team is part of the Biotech & Rare Disease (BRD) Manufacturing Development & Quality Control area that has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 500 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio.
Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact If you would like to know more about the position, please contact Director Alex Linnemann, on +45 34488105 Deadline 18 June 2023, but applicants are reviewed on an ongoing basis.
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.
In Biotech & Rare Diseases (BRD) expansion project in Måløv, we are planning to expand our production facilities. The aim of this new expansion project is to build a completely new manufacturing facility, including the implementation of isolator and other advanced technologies, with which Novo Nordisk has limited experience. This new facility aims to innovate our processes and to broaden our perspective, which is why this position requires a candidate with a good innovative mindset.
As our Operational Responsible for Formulation and Filtration, your main area of responsibility is getting processes and procedures ready for production.
Therefore, your main tasks will be:
• Responsible for filling all formulation and filtration activities.
• Project management and execution, including integration and cooperation with the program mirror organisation.
• Ensure that Systematic Problem Solving (SPS) and process confirmation are carried out in a structured way, and implementation of LEAN methodologies in the work carried out.
• Responsible for Quality and Compliance, ensuring that internal and internal quality demands comply to Current Good Manufacturing Practice (CGMP).
Though the project is located in Målev, interaction with the AP Expansion project on other sites is needed, and some travel or online-activity across the world, and time zones must be expected.
Qualifications To be considered for this position you have:
• An academic degree (BSc., MSc. or PhD.)
• Solid understanding of Current Good Manufacturing Practice (GMP)
• Preferably 5 years of project management experience, and/or Formulation and Filtration.
• Solid network within Product Supply (PS) and related areas within Novo Nordisk, or a lot of experience within the pharmaceutical industry.
• High verbal and written communication skills in English, plus good presentation skills. As a person, you have good cooperation and communications skills, and you are able to engage and coach own subordinates and other project team members. You are comfortable with working in an environment in constant change, with high complexity, and you are able to optimize, create and implement new working practices. You are result-oriented with a “can-do” attitude, being structured and organized with strong focus on high quality. About the Department Our team is part of the Biotech & Rare Disease (BRD) Manufacturing Development & Quality Control area that has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 500 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio.
Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact If you would like to know more about the position, please contact Director Alex Linnemann, on +45 34488105 Deadline 18 June 2023, but applicants are reviewed on an ongoing basis.
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 25.5.2023, 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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