Job Opportunities in Denmark
September 18, 2024
Novo Nordisk
Hillerød
Experienced IT/OT System Manager
Experienced IT/OT System Manager
Category: Digital & IT
Location: Hillerød, Capital Region of Denmark, DK
Are you motivated by working with global data collection and visualization solutions? Do you thrive as part of a diverse team with specialized competencies? Are you ready to embrace change in a dynamic work environment where no two days are the same? We are looking for an Experienced IT/OT System Manager within the Operational Technology (OT) Integration team in the Global Intralogistics & Future Operational Technologies (GILFOT) department to manage advanced solutions across the entire product cycle, from early development to global operation. Apply today for a life-changing career!
The Position
As an Experienced IT/OT System Manager, you will be responsible for the global operation and maintenance of data collection and visualization systems. You will be the main responsible for managing local infrastructure (Servers, AD, VMWare, Databases, LAN/VLAN, Backup/Restore) for the sites and will work closely with colleagues in Global IT operations and local IT departments at the production sites. Furthermore, you will be planning, driving and ensuring systematic periodic reviews are conducted timely and drive/report regarding Life Cycle Management, risk assessments, IT security planning, patching, user reviews in compliance with relevant requirements (c GMP, GAMP, 21CFR Part 11 and instructions).
Your role will include a variety of tasks such as:
As an Experienced IT/OT System Manager, you will be responsible for the global operation and maintenance of data collection and visualization systems. You will be the main responsible for managing local infrastructure (Servers, AD, VMWare, Databases, LAN/VLAN, Backup/Restore) for the sites and will work closely with colleagues in Global IT operations and local IT departments at the production sites. Furthermore, you will be planning, driving and ensuring systematic periodic reviews are conducted timely and drive/report regarding Life Cycle Management, risk assessments, IT security planning, patching, user reviews in compliance with relevant requirements (c GMP, GAMP, 21CFR Part 11 and instructions).
Your role will include a variety of tasks such as:
- Being IT compliance responsible of a standardized rollout plan for the solutions and writing and approving change requests, test protocols, and instructions
- Managing the operation and maintenance of global IT solutions and identifying new internal and external requirements
- Contributing to incident management and systematic problem-solving within an ITIL framework
- Executing quality activities such as IT risk assessments, qualification of the solutions and presenting IT systems during audits and inspections
- Coordinating activities with various stakeholders, managing system maintenance and changes, and offering advice and consultancy to IT and automation supporters
Qualifications
As our new colleague you fulfil several of the following qualifications:
As our new colleague you fulfil several of the following qualifications:
- Bachelor’s degree in computer science or information technology, and/or demonstrated experience in the field as an IT professional
- Ability to operate and maintain several systems in a structured way, keeping control in a highly regulated industry
- Proficient communication skills in both written and spoken English
- Experience with Service Now, ITIL, Veeva Vault, Octoplant, Linux (Red Hat Enterprise & Ubuntu), Virtualized environments, GMP and/or GAMP is considered advantage
On a personal level, your proficiency in conveying complex information to diverse audiences, ensuring stakeholder buy-in, will be pivotal in this role. Your ability to solve intricate problems and derive practical solutions, combined with a strong quality mindset and an analytical approach, will further underscore your suitability for this position.
About the department
Device Manufacturing Development (DMD) is responsible for the manufacturing development of all devices and packaging related processes at Novo Nordisk. We are an end-to-end corporate organisation developing products for high volume production, establishing control strategy of the product, developing, and implementing the production equipment at the production site all over the world, and developing innovative and digital solutions to our processes.
Device Manufacturing Development (DMD) is responsible for the manufacturing development of all devices and packaging related processes at Novo Nordisk. We are an end-to-end corporate organisation developing products for high volume production, establishing control strategy of the product, developing, and implementing the production equipment at the production site all over the world, and developing innovative and digital solutions to our processes.
Within DMD, this position is located in the Global IL & Future Operational Technologies department, which explores manufacturing and operational technologies and transforms them into applicable solutions and standards used for enhancing production capacity and operational effectiveness.
Our department is highly motivated, and this position offers you a unique opportunity to use and strengthen your leadership skills in an exciting environment together with great employees and colleagues. You will experience an enthusiastic working climate where we take personal responsibility for quality, delivery, and each other.
Working at FPM, Novo Nordisk
Finished Product Manufacturing (FPM) is a part of Novo Nordisk Product Supply, a global production network at the forefront of technology and quality production of pharmaceutical products. At FPM, we not only manufacture all finished products for people living with serious chronic diseases, we also use our competencies to drive technology leadership and improve standards across our core technologies to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
Our global network consists of around 6,000 colleagues across ten countries. Here, we are responsible for the manufacturing of all finished products, including devices, needles, assembly, and packaging. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we strive to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.
Working at FPM, Novo Nordisk
Finished Product Manufacturing (FPM) is a part of Novo Nordisk Product Supply, a global production network at the forefront of technology and quality production of pharmaceutical products. At FPM, we not only manufacture all finished products for people living with serious chronic diseases, we also use our competencies to drive technology leadership and improve standards across our core technologies to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
Our global network consists of around 6,000 colleagues across ten countries. Here, we are responsible for the manufacturing of all finished products, including devices, needles, assembly, and packaging. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we strive to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.
Contact
For further information, please contact Mads Hjertstedt, Senior Development Engineer on +4534481394.
For further information, please contact Mads Hjertstedt, Senior Development Engineer on +4534481394.
Deadline
29 September 2024.
29 September 2024.
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate has been identified. 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.
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