Novartis Radiopharmaceuticals GmbH
ITOT Specialist(m/w/x)
Full-timeOn-siteSenior
Halle (Saale)
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On-site ITOT lead for new Radioligand Therapy manufacturing site build-out. GMP validation and testing experience required. Relocation support unavailable, support for applicants with disabilities.
Requirements
- Bachelor's degree in engineering, IT, or computer science
- At least five years of IT or 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 or 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 on-site ITOT lead for site build-out
- Coordinate ITOT suppliers and partners during construction
- Lead validation and testing activities
- Ensure traceability from requirements to system delivery
- Partner with leadership and engineering on capital projects
- Deliver capital projects on time and to quality
- Ensure compliance with HSE standards
- Support transition to stable operations
- Enable reliable day-to-day site performance
- Communicate progress, risks, and priorities
- Communicate to senior stakeholders and teams
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Other Benefits
- Relocation support unavailable
- Support for applicants with disabilities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis 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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On-site ITOT lead for new Radioligand Therapy manufacturing site build-out. GMP validation and testing experience required. Relocation support unavailable, support for applicants with disabilities.
Requirements
- Bachelor's degree in engineering, IT, or computer science
- At least five years of IT or 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 or 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 on-site ITOT lead for site build-out
- Coordinate ITOT suppliers and partners during construction
- Lead validation and testing activities
- Ensure traceability from requirements to system delivery
- Partner with leadership and engineering on capital projects
- Deliver capital projects on time and to quality
- Ensure compliance with HSE standards
- Support transition to stable operations
- Enable reliable day-to-day site performance
- Communicate progress, risks, and priorities
- Communicate to senior stakeholders and teams
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Other Benefits
- Relocation support unavailable
- Support for applicants with disabilities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis 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
Industry
Pharmaceuticals
Description
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Not a perfect match?
- Novartis Radiopharmaceuticals GmbH
ITOT Specialist(m/w/x)
Full-timeOn-siteSeniorHalle (Saale) - Novartis Radiopharmaceuticals GmbH
Process Expert(m/w/x)
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Spezialist Automatisierungstechnik(m/w/x)
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