Dein persönlicher KI-Karriere-Agent
ITOT Specialist(m/w/x)
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Benefits
Sonstige Vorteile
- Relocation support unavailable
- Support for applicants with disabilities
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ITOT Specialist(m/w/x)
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Benefits
Sonstige Vorteile
- Relocation support unavailable
- Support for applicants with disabilities
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Novartis
Branche
Pharmaceuticals
Beschreibung
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Noch nicht perfekt?
- Novartis Radiopharmaceuticals GmbH
ITOT Specialist(m/w/x)
Vollzeitnur vor OrtSeniorHalle (Saale) - Novartis Radiopharmaceuticals GmbH
Project Director(m/w/x)
Vollzeitnur vor OrtSeniorHalle (Saale) - Novartis Radiopharmaceuticals GmbH
Process Expert(m/w/x)
Vollzeitnur vor OrtBerufserfahrenHalle (Saale) - Simtra BioPharma Solutions
Spezialist Inprozesskontrolle(m/w/x)
Vollzeitnur vor OrtBerufserfahrenHalle (Saale) - Simtra BioPharma Solutions
Specialist Project Validation(m/w/x)
Vollzeitnur vor OrtBerufserfahrenHalle (Saale)