Manufacturing Execution System User
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Måløv
Do you have experience within Manufacturing Execution Systems (MES) and possibly knowledge of Good Practices and pharmaceutical production? Are you passionate about data, technology and digitalization? Are you motivated to use your technical skills to collect and analyse data to develop excellent standardized and integrated IT solutions in our MES system?
If so apply today if you want to be part of a life-changing career!
The position
In this job, you will be responsible for the creation and the continuous improvement of our master batch records in PAS-X, thereby optimizing the digitalization of our manufacturing processes.
Among other tasks you will:
• have the responsibility of implementing and validating the new and improved digital solutions
• ensure the creation and update of master data and assist in systemic troubleshooting before, during, and after productions
• be part of building and maintaining a robust digital foundation
• be responsible for increasing the department knowledge about our MES system, e.g. through training and communication about the changes and updates you make
Moreover, you will be responsible for the prioritizing among and implementation of new and improved solutions based on project needs and inputs from the MES users (manufacturing supporters, technicians and operators) in order to ensure that we are ready for production of new development products as well as ensuring that our clinical productions are running smoothly.
In your daily work, you will have many stakeholders across the organization including production, development, business support, IT, and QA. Your working day will be versatile, and your tasks will have short as well as long deadlines.
Qualifications
In order to succeed in this role you:
• have a relevant academic background, e.g., software-, mechanical-, chemical, or production engineering, or other relevant education
• have experience with MES as a consultant, developer, superuser, or similar
• have experience from GxP regulated production environment
It is an advantage if you have worked with PAS-X and/or SAP and worked with the validation of systems, master data or pharmaceutical manufacturing
On a personal level you are good at keeping the overview and enjoy collaboration with several stakeholders.
Moreover, you possess good communication skills in both oral and written English. You thrive in a dynamic environment; you are comfortable with a high pace, and you have a positive can-do attitude.
About the department
Oral Finished Products (OFP) MDev Operations employs app. 80 highly skilled and motivated employees with the mission to bring oral products from late-stage development to market production. The department aid the process development work of all new oral project and is responsible for the manufacture and packing of oral drug products for all phase 3 clinical trials. Our production facility is used for development studies as well as clinical and commercial manufacturing.
Our ambition is to bring breakthrough oral products from late-stage development to commercial production!
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 PAS-X & SAP Area Responsible Super User Ermira Adrovic, +4530794880, or Associate Manager Benedikte Yding Schneller, +4530794037.
Deadline
31 December 2022
Applications will be reviewed on an ongoing basis, so please do apply as soon as possible!
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
#LI-AMS1
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.
Print job Send to e-mail
If so apply today if you want to be part of a life-changing career!
The position
In this job, you will be responsible for the creation and the continuous improvement of our master batch records in PAS-X, thereby optimizing the digitalization of our manufacturing processes.
Among other tasks you will:
• have the responsibility of implementing and validating the new and improved digital solutions
• ensure the creation and update of master data and assist in systemic troubleshooting before, during, and after productions
• be part of building and maintaining a robust digital foundation
• be responsible for increasing the department knowledge about our MES system, e.g. through training and communication about the changes and updates you make
Moreover, you will be responsible for the prioritizing among and implementation of new and improved solutions based on project needs and inputs from the MES users (manufacturing supporters, technicians and operators) in order to ensure that we are ready for production of new development products as well as ensuring that our clinical productions are running smoothly.
In your daily work, you will have many stakeholders across the organization including production, development, business support, IT, and QA. Your working day will be versatile, and your tasks will have short as well as long deadlines.
Qualifications
In order to succeed in this role you:
• have a relevant academic background, e.g., software-, mechanical-, chemical, or production engineering, or other relevant education
• have experience with MES as a consultant, developer, superuser, or similar
• have experience from GxP regulated production environment
It is an advantage if you have worked with PAS-X and/or SAP and worked with the validation of systems, master data or pharmaceutical manufacturing
On a personal level you are good at keeping the overview and enjoy collaboration with several stakeholders.
Moreover, you possess good communication skills in both oral and written English. You thrive in a dynamic environment; you are comfortable with a high pace, and you have a positive can-do attitude.
About the department
Oral Finished Products (OFP) MDev Operations employs app. 80 highly skilled and motivated employees with the mission to bring oral products from late-stage development to market production. The department aid the process development work of all new oral project and is responsible for the manufacture and packing of oral drug products for all phase 3 clinical trials. Our production facility is used for development studies as well as clinical and commercial manufacturing.
Our ambition is to bring breakthrough oral products from late-stage development to commercial production!
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 PAS-X & SAP Area Responsible Super User Ermira Adrovic, +4530794880, or Associate Manager Benedikte Yding Schneller, +4530794037.
Deadline
31 December 2022
Applications will be reviewed on an ongoing basis, so please do apply as soon as possible!
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
#LI-AMS1
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.
Print job Send to e-mail
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 5.8.2022, 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
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