IT System Manager
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Måløv
IT System Manager/IT Administrator role in CMC Oral Protein Development On the edge of the future
Come and join a department who are frontrunners in Novo Nordisk in relation to digitalisation, future manufacturing processes and risk-based decision making. As a team member you enjoy working in an open, dynamic and social atmosphere with a strong focus on technical and scientific skills. Your team consists of 11 dedicated colleagues maintaining the overall IT infrastructure and compliance of various systems within production and production development within the R&D family in Novo Nordisk.
About the department
As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (CMC) Development makes a real difference for patients with chronic diseases across the world. We develop and formulate all new processes coming out of our research units in our pilot plants, ensuring that we bring best-in-class treatments to the market. The Oral Protein Development (OPDev) is an area within CMC Development, which employs approximately 220 highly skilled people organised in five departments and is based in Måløv. Our focus is to develop and manufacture solid dose tablets for pre-clinical and clinical trial phases I and II covering a broad and exciting range of process technologies for solid dosage forms. The position
You will join the department - OPDev Technical support – which consists of two teams, contributing with a broad range of skills, such as maintenance, calibration, qualification, IT and general support to ensure daily operations of GsP and GmP IT systems. You will be a part of our IT & Quality team. As IT system Manager, you will be responsible for the operation and maintenance of several GxP critical IT systems located and used in OPDev during their full life-cycle. As equipment and processes are developed and optimized, you need to ensure that all our systems always follow Novo Nordisk’s procedures and external guidelines for computer systems validation (e.g. GAMP) and that we are ready to meet the standards of the future. To achieve that, you:
Continuously plan and perform validation activities, provide maintenance support to the process IT systems currently used within the area, including user administration, ensure IT security and data integrity.
Drive implementation of IT system upgrades and new process IT systems. Implement IT systems/-solutions together with other IT Validation Managers to ensure appropriate test protocols and documentation standards are met.
You will work closely with an IT sub-team – IT System managers, IT Administrators, IT/OT Engineers and IT Partner - where teamwork is a key value, and planning and coordination is a must, to be able to succeed in a dynamic environment. Across your tasks and projects, you will also have a close collaboration with stakeholders such as End-users, Project managers, Quality Assurance and Process Groups, but most of all, our team, ensuring that our project timelines and deliverables are met.
Qualifications
You hold a relevant educational background e.g. Bachelor, Masters or equivalent in engineering or IT optimally combined with a few years of relevant working experience, which has given you a solid analytic approach to problem solving. Ideally you have both Knowledge of IT security and networks and knowledge of compliance within IT systems in the pharmaceutical industry as well as experience in supporting, configuring and maintaining such systems. As a person, you
• dare to take the lead, even when the task initially is a bit blurry.
• have a strong quality mind-set in general, and specifically in documentation/validation.
• enjoy providing daily support within your area of expertise to end-users.
• like working together with stakeholders of different professions
• are thorough and find it natural to work independently.
• Are a good communicator, who shares knowledge to strengthen the overall abilities of our team and you are proficient in both English and Danish or another Scandinavian language.
Contact
For further information, please contact IT Partner, Rasmus Thue Elkjær Dvinge +45 30775097 or Associate Manager, Nicolai Kristensen at +45 30753501
Deadline
16th of April 2023
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
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.
Come and join a department who are frontrunners in Novo Nordisk in relation to digitalisation, future manufacturing processes and risk-based decision making. As a team member you enjoy working in an open, dynamic and social atmosphere with a strong focus on technical and scientific skills. Your team consists of 11 dedicated colleagues maintaining the overall IT infrastructure and compliance of various systems within production and production development within the R&D family in Novo Nordisk.
About the department
As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (CMC) Development makes a real difference for patients with chronic diseases across the world. We develop and formulate all new processes coming out of our research units in our pilot plants, ensuring that we bring best-in-class treatments to the market. The Oral Protein Development (OPDev) is an area within CMC Development, which employs approximately 220 highly skilled people organised in five departments and is based in Måløv. Our focus is to develop and manufacture solid dose tablets for pre-clinical and clinical trial phases I and II covering a broad and exciting range of process technologies for solid dosage forms. The position
You will join the department - OPDev Technical support – which consists of two teams, contributing with a broad range of skills, such as maintenance, calibration, qualification, IT and general support to ensure daily operations of GsP and GmP IT systems. You will be a part of our IT & Quality team. As IT system Manager, you will be responsible for the operation and maintenance of several GxP critical IT systems located and used in OPDev during their full life-cycle. As equipment and processes are developed and optimized, you need to ensure that all our systems always follow Novo Nordisk’s procedures and external guidelines for computer systems validation (e.g. GAMP) and that we are ready to meet the standards of the future. To achieve that, you:
Continuously plan and perform validation activities, provide maintenance support to the process IT systems currently used within the area, including user administration, ensure IT security and data integrity.
Drive implementation of IT system upgrades and new process IT systems. Implement IT systems/-solutions together with other IT Validation Managers to ensure appropriate test protocols and documentation standards are met.
You will work closely with an IT sub-team – IT System managers, IT Administrators, IT/OT Engineers and IT Partner - where teamwork is a key value, and planning and coordination is a must, to be able to succeed in a dynamic environment. Across your tasks and projects, you will also have a close collaboration with stakeholders such as End-users, Project managers, Quality Assurance and Process Groups, but most of all, our team, ensuring that our project timelines and deliverables are met.
Qualifications
You hold a relevant educational background e.g. Bachelor, Masters or equivalent in engineering or IT optimally combined with a few years of relevant working experience, which has given you a solid analytic approach to problem solving. Ideally you have both Knowledge of IT security and networks and knowledge of compliance within IT systems in the pharmaceutical industry as well as experience in supporting, configuring and maintaining such systems. As a person, you
• dare to take the lead, even when the task initially is a bit blurry.
• have a strong quality mind-set in general, and specifically in documentation/validation.
• enjoy providing daily support within your area of expertise to end-users.
• like working together with stakeholders of different professions
• are thorough and find it natural to work independently.
• Are a good communicator, who shares knowledge to strengthen the overall abilities of our team and you are proficient in both English and Danish or another Scandinavian language.
Contact
For further information, please contact IT Partner, Rasmus Thue Elkjær Dvinge +45 30775097 or Associate Manager, Nicolai Kristensen at +45 30753501
Deadline
16th of April 2023
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
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 29.3.2023, 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
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