Manufacturing Execution System Specialist
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Måløv
Does it excite you to drive change by being at the forefront of modern technology and IT? Does your expertise cover handling of Manufacturing Execution System (MES) activities in a GMP regulated production environment? Are you driven by ensuring high quality and high customer satisfaction in your daily work?
Then come and join us as our new MES Specialist, apply now!
The position
As a MES Specialist, you will play a key role in our PAS-X project teams in OFP, where we support our production in delivering tablets to patients globally. The position requires the ability to take decisions based on business requirements and business strategy and our overall aim is to improve the efficiency of all manufacturing-related processes.
Your main responsibilities will be to:
• Analysing production processes, and designing, describing, and testing MES changes in collaboration with OFP production
• Mentoring colleagues in the team and OFP
• Eliminate production issues in relation to PAS-X and PAS-X barcode equipment in our production facilities
The existing PAS-X team consists of 6 dedicated people who have established a strong culture around trust, responsibility, fun and helping each other.
Qualifications
To succeed in this job, you should love to bridge your technical MES knowledge with local business process requirements to identify and collect data, make a structured analysis, and develop excellent standardized and integrated IT solutions in PAS-X.
The qualifications we are looking for are:
• Master’s degree within a relevant discipline e.g., Engineering, business, economics, pharmacist or equivalent
• Ideally 5+ years of experience of MES or other related systems, preferably PAS-X or MBR design; experience with production line/equipment integration is preferred
• Strong communication skills both written and orally
• Full English proficiency
Experience with GMP validation of IT systems in a regulated production environment, such as the pharmaceutical industry, is highly beneficial and will be seen as an advantage.
As a person, you are a strong individual who can come up with innovative solutions and have the ability to demonstrate a capacity for gathering requirements to identify issues, opportunities, and patterns. You have a flair for stakeholder management and the ability to be self-motivated, structured, and targeted having a high degree of flexibility.
Your empathy and IT apprehension guide you to transform complex technical challenges and demands into workable solutions. This position requires strong commitment and the ability to make decisions, often in a high-pressure, consensus-driven and political environment. About The Department
You will be part of the IT department, consisting of 30 dedicated people split into 2 teams. We are responsible for IT compliance and productions systems in OFP in Måløv which is a part of Product Supply in Novo Nordisk. You will join our team of PAS-X professionals and specialists who participate in analysing production processes, and who configure and implement solutions in the MES PAS-X, in close cooperation with all other areas on our site such as bulk, pack and QA. In our team there is a great atmosphere and team spirit, and we are a group of people with various backgrounds, but we all have in common that we want to support and help each other, have a good time, and make a big difference. 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
For further information, please contact Randi Skjøtt +45 3448 1149
Deadline
18 June 2023 Applications and interviews will be screened and held on an ongoing basis, so you are encouraged to 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.
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.
Then come and join us as our new MES Specialist, apply now!
The position
As a MES Specialist, you will play a key role in our PAS-X project teams in OFP, where we support our production in delivering tablets to patients globally. The position requires the ability to take decisions based on business requirements and business strategy and our overall aim is to improve the efficiency of all manufacturing-related processes.
Your main responsibilities will be to:
• Analysing production processes, and designing, describing, and testing MES changes in collaboration with OFP production
• Mentoring colleagues in the team and OFP
• Eliminate production issues in relation to PAS-X and PAS-X barcode equipment in our production facilities
The existing PAS-X team consists of 6 dedicated people who have established a strong culture around trust, responsibility, fun and helping each other.
Qualifications
To succeed in this job, you should love to bridge your technical MES knowledge with local business process requirements to identify and collect data, make a structured analysis, and develop excellent standardized and integrated IT solutions in PAS-X.
The qualifications we are looking for are:
• Master’s degree within a relevant discipline e.g., Engineering, business, economics, pharmacist or equivalent
• Ideally 5+ years of experience of MES or other related systems, preferably PAS-X or MBR design; experience with production line/equipment integration is preferred
• Strong communication skills both written and orally
• Full English proficiency
Experience with GMP validation of IT systems in a regulated production environment, such as the pharmaceutical industry, is highly beneficial and will be seen as an advantage.
As a person, you are a strong individual who can come up with innovative solutions and have the ability to demonstrate a capacity for gathering requirements to identify issues, opportunities, and patterns. You have a flair for stakeholder management and the ability to be self-motivated, structured, and targeted having a high degree of flexibility.
Your empathy and IT apprehension guide you to transform complex technical challenges and demands into workable solutions. This position requires strong commitment and the ability to make decisions, often in a high-pressure, consensus-driven and political environment. About The Department
You will be part of the IT department, consisting of 30 dedicated people split into 2 teams. We are responsible for IT compliance and productions systems in OFP in Måløv which is a part of Product Supply in Novo Nordisk. You will join our team of PAS-X professionals and specialists who participate in analysing production processes, and who configure and implement solutions in the MES PAS-X, in close cooperation with all other areas on our site such as bulk, pack and QA. In our team there is a great atmosphere and team spirit, and we are a group of people with various backgrounds, but we all have in common that we want to support and help each other, have a good time, and make a big difference. 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
For further information, please contact Randi Skjøtt +45 3448 1149
Deadline
18 June 2023 Applications and interviews will be screened and held on an ongoing basis, so you are encouraged to 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.
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 22.5.2023, 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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