Dein persönlicher KI-Karriere-Agent
Application Owner (GxP / Validated Systems)(m/w/x)
Managing full lifecycle of GxP-validated applications for rare disease therapies at a critical care provider. Several years of GxP IT application management experience and hands-on CSV expertise required. Vendor relationship management and incident coordination.
Anforderungen
- Degree in IT, Life Sciences, Engineering, or related field
- Several years of IT application management experience in GxP-regulated environment
- Hands-on CSV expertise
- Strong knowledge of EU GMP Annex 11, 21 CFR Part 11, GAMP 5
- Strong knowledge of risk-based validation and change control approaches
- Experience supporting audits and inspections
- Proven experience collaborating with external software vendors
- Advantageous: ISPE certification (CPGP) or GAMP 5 training
- Plus: ASQ certifications (CQA or CQE)
- Beneficial: ITIL Foundation certification
- Experience with ERP, QMS, LIMS, or document management systems in regulated environments
- Experience with SaaS/cloud validation
- Background in pharmaceutical, biotech, or medical device industries
- Strong understanding of data integrity and security principles
- Experience working in complex, fast-paced environments
- Experience driving organizational change
- Familiarity with ITIL and service management principles
- Experience with Agile and/or DevOps methodologies
- Degree in IT, Life Sciences, Engineering, or related field
- Several years of IT application management experience in GxP-regulated environment
- Hands-on CSV expertise
- Strong knowledge of EU GMP Annex 11, 21 CFR Part 11, GAMP 5
- Strong knowledge of risk-based validation and change control approaches
- Experience supporting audits and inspections
- Proven experience collaborating with external software vendors
- Advantageous: ISPE certification (CPGP) or GAMP 5 training
- Plus: ASQ certifications (CQA or CQE)
- Beneficial: ITIL Foundation certification
- Experience with ERP, QMS, LIMS, or document management systems in regulated environments
- Experience with SaaS/cloud validation
- Background in pharmaceutical, biotech, or medical device industries
- Strong understanding of data integrity and security principles
- Experience working in complex, fast-paced environments
- Experience driving organizational change
- Familiarity with ITIL and service management principles
- Experience with Agile and/or DevOps methodologies
Aufgaben
- Serve as the key interface between IT, QA, business stakeholders, and external vendors.
- Manage the full application lifecycle.
- Ensure reliable application performance and availability.
- Ensure compliant application upgrades and releases.
- Manage vendor relationships, SLAs, and support contracts.
- Coordinate incident, problem, and change management processes.
- Ensure validated systems remain compliant throughout their lifecycle.
- Oversee risk-based (GAMP 5) validation activities.
- Perform change impact assessments.
- Manage required validation documentation.
- Support audits and inspections.
- Conduct periodic system reviews.
- Ensure alignment with EU GMP Annex 11, 21 CFR Part 11, and ALCOA+ principles.
- Perform and document risk assessments.
- Ensure proper access management.
- Ensure segregation of duties.
- Maintain full traceability across requirements, testing, and validation documentation.
- Collaborate with QA on compliance expectations.
- Support continuous improvement of validation and governance processes.
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- CSV
- EU GMP Annex 11
- 21 CFR Part 11
- GAMP 5
- ITIL
- ERP
- QMS
- LIMS
- SaaS
- Cloud validation
Benefits
Lockere Unternehmenskultur
- Open corporate culture
- Collegial and committed team
Sinnstiftende Arbeit
- Opportunity to contribute ideas
- Independent work
Modernes Büro
- Modern working environment
Parkplatz & Pendelvorteile
- Good public transport connections
- Parking spot
Flexibles Arbeiten
- Flexible working hours
- Home office
Boni & Prämien
- Bonus
Team Events & Ausflüge
- Employee events
Mentoring & Coaching
- Structured onboarding
- Buddy system support
Moderne Technikausstattung
- Employee mobile phone
- Laptop
Weiterbildungsangebote
- Initial and continuing education
Gratis oder Vergünstigte Mahlzeiten
- Canteen
Sonstige Zulagen
- Meal allowance
Gesundheits- & Fitnessangebote
- Company doctor
- Health measures
Mitarbeiterrabatte
- Employee discount
Firmenwagen
- Company car
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Noch nicht perfekt?
- AOP HealthVollzeitmit HomeofficeSeniorWienab 45.080 / Jahr
- Mundipharma Gesellschaft .m.b.H.
Associate Quality Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 2.986 / Monat - Takeda Manufacturing Austria AG
Validation Specialist BioLife Laboratory Information Management System(m/w/x)
Vollzeitmit HomeofficeJuniorWienab 4.270,14 / Monat - AOP Health
Senior Associate Serialization(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - MUELLBACHER Personalberatung
IT Applikationsbetreuer:in Laborinformationssysteme (LIS)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 3.800 / Monat
Application Owner (GxP / Validated Systems)(m/w/x)
Managing full lifecycle of GxP-validated applications for rare disease therapies at a critical care provider. Several years of GxP IT application management experience and hands-on CSV expertise required. Vendor relationship management and incident coordination.
Anforderungen
- Degree in IT, Life Sciences, Engineering, or related field
- Several years of IT application management experience in GxP-regulated environment
- Hands-on CSV expertise
- Strong knowledge of EU GMP Annex 11, 21 CFR Part 11, GAMP 5
- Strong knowledge of risk-based validation and change control approaches
- Experience supporting audits and inspections
- Proven experience collaborating with external software vendors
- Advantageous: ISPE certification (CPGP) or GAMP 5 training
- Plus: ASQ certifications (CQA or CQE)
- Beneficial: ITIL Foundation certification
- Experience with ERP, QMS, LIMS, or document management systems in regulated environments
- Experience with SaaS/cloud validation
- Background in pharmaceutical, biotech, or medical device industries
- Strong understanding of data integrity and security principles
- Experience working in complex, fast-paced environments
- Experience driving organizational change
- Familiarity with ITIL and service management principles
- Experience with Agile and/or DevOps methodologies
- Degree in IT, Life Sciences, Engineering, or related field
- Several years of IT application management experience in GxP-regulated environment
- Hands-on CSV expertise
- Strong knowledge of EU GMP Annex 11, 21 CFR Part 11, GAMP 5
- Strong knowledge of risk-based validation and change control approaches
- Experience supporting audits and inspections
- Proven experience collaborating with external software vendors
- Advantageous: ISPE certification (CPGP) or GAMP 5 training
- Plus: ASQ certifications (CQA or CQE)
- Beneficial: ITIL Foundation certification
- Experience with ERP, QMS, LIMS, or document management systems in regulated environments
- Experience with SaaS/cloud validation
- Background in pharmaceutical, biotech, or medical device industries
- Strong understanding of data integrity and security principles
- Experience working in complex, fast-paced environments
- Experience driving organizational change
- Familiarity with ITIL and service management principles
- Experience with Agile and/or DevOps methodologies
Aufgaben
- Serve as the key interface between IT, QA, business stakeholders, and external vendors.
- Manage the full application lifecycle.
- Ensure reliable application performance and availability.
- Ensure compliant application upgrades and releases.
- Manage vendor relationships, SLAs, and support contracts.
- Coordinate incident, problem, and change management processes.
- Ensure validated systems remain compliant throughout their lifecycle.
- Oversee risk-based (GAMP 5) validation activities.
- Perform change impact assessments.
- Manage required validation documentation.
- Support audits and inspections.
- Conduct periodic system reviews.
- Ensure alignment with EU GMP Annex 11, 21 CFR Part 11, and ALCOA+ principles.
- Perform and document risk assessments.
- Ensure proper access management.
- Ensure segregation of duties.
- Maintain full traceability across requirements, testing, and validation documentation.
- Collaborate with QA on compliance expectations.
- Support continuous improvement of validation and governance processes.
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- CSV
- EU GMP Annex 11
- 21 CFR Part 11
- GAMP 5
- ITIL
- ERP
- QMS
- LIMS
- SaaS
- Cloud validation
Benefits
Lockere Unternehmenskultur
- Open corporate culture
- Collegial and committed team
Sinnstiftende Arbeit
- Opportunity to contribute ideas
- Independent work
Modernes Büro
- Modern working environment
Parkplatz & Pendelvorteile
- Good public transport connections
- Parking spot
Flexibles Arbeiten
- Flexible working hours
- Home office
Boni & Prämien
- Bonus
Team Events & Ausflüge
- Employee events
Mentoring & Coaching
- Structured onboarding
- Buddy system support
Moderne Technikausstattung
- Employee mobile phone
- Laptop
Weiterbildungsangebote
- Initial and continuing education
Gratis oder Vergünstigte Mahlzeiten
- Canteen
Sonstige Zulagen
- Meal allowance
Gesundheits- & Fitnessangebote
- Company doctor
- Health measures
Mitarbeiterrabatte
- Employee discount
Firmenwagen
- Company car
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
AOP Health
Branche
Pharmaceuticals
Beschreibung
AOP Health is the European pioneer for integrated therapies for rare diseases and in critical care.
Noch nicht perfekt?
- AOP Health
Application Owner – Veeva Platform(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - Mundipharma Gesellschaft .m.b.H.
Associate Quality Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 2.986 / Monat - Takeda Manufacturing Austria AG
Validation Specialist BioLife Laboratory Information Management System(m/w/x)
Vollzeitmit HomeofficeJuniorWienab 4.270,14 / Monat - AOP Health
Senior Associate Serialization(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - MUELLBACHER Personalberatung
IT Applikationsbetreuer:in Laborinformationssysteme (LIS)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 3.800 / Monat