Novartis
ITOT Specialist(m/w/x)
Full-timeOn-siteSenior
Halle (Saale)
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NONovartis Radiopharmaceuticals GmbH
ITOT Specialist(m/w/x)
Halle (Saale)
Full-timeOn-siteSenior
Nejo AI Summary
Establishing compliant IT/OT systems for new Radioligand Therapy manufacturing site. Five years IT/OT experience in regulated industries required. Relocation support unavailable.
Requirements
- Bachelor's degree in engineering, IT, or computer science
- At least five years of IT/OT experience in regulated industries
- Proven experience supporting site build, capital projects, or system implementation
- Strong knowledge of validation, testing, and compliance in GMP environments
- Ability to lead stakeholders, manage suppliers, and influence without authority
- Fluency in English and German, strong communication and stakeholder engagement skills
- Experience in pharmaceutical or automotive environments with system validation
- Bachelor's degree in engineering, IT, or computer science
- At least five years of IT/OT experience in regulated industries
- Proven experience supporting site build, capital projects, or system implementation
- Strong knowledge of validation, testing, and compliance in GMP environments
- Ability to lead stakeholders, manage suppliers, and influence without authority
- Fluency in English and German, strong communication and stakeholder engagement skills
- Experience in pharmaceutical or automotive environments with system validation
- Analytical thinking
- Business acumen
- Communication skills
- Digital capabilities
- Effective use of technology
- Requirements analysis
- Requirements gathering
- Stakeholder management
Tasks
- Act as the on-site ITOT lead for site build-out
- Coordinate ITOT suppliers and partners during construction
- Coordinate ITOT suppliers and partners during installation
- Coordinate ITOT suppliers and partners during commissioning
- Lead validation activities
- Lead testing activities
- Ensure traceability from user requirements to system delivery
- Partner with site leadership to deliver capital projects
- Partner with engineering teams to deliver capital projects
- Ensure compliance with security standards
- Ensure compliance with quality standards
- Ensure compliance with health standards
- Ensure compliance with safety standards
- Ensure compliance with environmental standards
- Support transition to stable operations
- Enable reliable day-to-day site performance
- Communicate progress to senior stakeholders
- Communicate risks to senior stakeholders
- Communicate priorities to senior stakeholders
- Communicate progress to cross-functional teams
- Communicate risks to cross-functional teams
- Communicate priorities to cross-functional teams
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Other Benefits
- Relocation support unavailable
- Support for disabled applicants
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Radiopharmaceuticals GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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NONovartis Radiopharmaceuticals GmbH
ITOT Specialist(m/w/x)
Halle (Saale)
Full-timeOn-siteSenior
Nejo AI Summary
Establishing compliant IT/OT systems for new Radioligand Therapy manufacturing site. Five years IT/OT experience in regulated industries required. Relocation support unavailable.
Requirements
- Bachelor's degree in engineering, IT, or computer science
- At least five years of IT/OT experience in regulated industries
- Proven experience supporting site build, capital projects, or system implementation
- Strong knowledge of validation, testing, and compliance in GMP environments
- Ability to lead stakeholders, manage suppliers, and influence without authority
- Fluency in English and German, strong communication and stakeholder engagement skills
- Experience in pharmaceutical or automotive environments with system validation
- Bachelor's degree in engineering, IT, or computer science
- At least five years of IT/OT experience in regulated industries
- Proven experience supporting site build, capital projects, or system implementation
- Strong knowledge of validation, testing, and compliance in GMP environments
- Ability to lead stakeholders, manage suppliers, and influence without authority
- Fluency in English and German, strong communication and stakeholder engagement skills
- Experience in pharmaceutical or automotive environments with system validation
- Analytical thinking
- Business acumen
- Communication skills
- Digital capabilities
- Effective use of technology
- Requirements analysis
- Requirements gathering
- Stakeholder management
Tasks
- Act as the on-site ITOT lead for site build-out
- Coordinate ITOT suppliers and partners during construction
- Coordinate ITOT suppliers and partners during installation
- Coordinate ITOT suppliers and partners during commissioning
- Lead validation activities
- Lead testing activities
- Ensure traceability from user requirements to system delivery
- Partner with site leadership to deliver capital projects
- Partner with engineering teams to deliver capital projects
- Ensure compliance with security standards
- Ensure compliance with quality standards
- Ensure compliance with health standards
- Ensure compliance with safety standards
- Ensure compliance with environmental standards
- Support transition to stable operations
- Enable reliable day-to-day site performance
- Communicate progress to senior stakeholders
- Communicate risks to senior stakeholders
- Communicate priorities to senior stakeholders
- Communicate progress to cross-functional teams
- Communicate risks to cross-functional teams
- Communicate priorities to cross-functional teams
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Other Benefits
- Relocation support unavailable
- Support for disabled applicants
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Radiopharmaceuticals GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Novartis Radiopharmaceuticals GmbH
Industry
Pharmaceuticals
Description
Novartis Radiopharmaceuticals GmbH is a manufacturing plant for Radioligand Therapy (RLT) drug products.
Not a perfect match?
- Novartis
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Full-timeOn-siteSeniorHalle (Saale) - Novartis Radiopharmaceuticals GmbH
Project Director(m/w/x)
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Process Expert(m/w/x)
Full-timeOn-siteExperiencedHalle (Saale) - Simtra BioPharma Solutions
Spezialist Inprozesskontrolle(m/w/x)
Full-timeOn-siteExperiencedHalle (Saale) - Simtra BioPharma Solutions
Spezialist Automatisierungstechnik(m/w/x)
Full-timeOn-siteSeniorHalle (Saale)