Dein persönlicher KI-Karriere-Agent
R&D Quality Lead(m/w/x)
Oversight of R&D quality assurance and compliance for health authority regulations. GxP and cGMP experience required. Support for applicants with disabilities.
Anforderungen
- Audit & Inspection Management
- Quality Management Systems
- Quality Assurance
- GxP Experience
- Good Manufacturing Practices (cGMP)
- People Management
- Quality Compliance
- Drug Development
- Research
- Technological Expertise
- Complaints Management
- Good Laboratory Practice (GLP) Analytics
- Incident Management
- Deviation Management
- Patient Safety
- Pharmacovigilance
- English proficiency
Aufgaben
- Provide quality assurance and compliance oversight
- Drive quality management systems and initiatives
- Ensure compliance with health authority regulations
- Role model good quality behaviors
- Promote a culture of quality
- Develop and support quality plan initiatives
- Provide QA expertise and guidance
- Implement quality risk-based and GxP processes
- Lead and manage a QA organization
- Collaborate with business partners and quality groups
- Translate QA strategy into operational activities
- Support risk-based process implementation
- Address and sustain quality and compliance gaps
- Implement strategic process improvements
- Review procedural updates and training
- Conduct effectiveness checks
- Monitor Quality Plan implementation
- Support inspection readiness activities
- Participate in regulatory inspections
- Manage inspection preparation and follow-up
- Oversee external service providers and IT systems
- Facilitate and follow up on audits and inspections
- Develop and implement corrective and preventive measures
- Escalate deviations and incidents timely
- Conduct robust investigations and root cause analysis
- Implement corrective actions
- Contribute to lessons learned
- Report technical complaints and adverse events within 24 hours
- Distribute marketing samples where applicable
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – fließend
Benefits
Sonstige Vorteile
- Adjustments for applicants with disabilities
- Involvement of local disability representative (BVP)
Abwechslungsreiche Aufgaben
- Advice on suitable positions
Mentoring & Coaching
- Guidance at all stages of the application process
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
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R&D Quality Lead(m/w/x)
Oversight of R&D quality assurance and compliance for health authority regulations. GxP and cGMP experience required. Support for applicants with disabilities.
Anforderungen
- Audit & Inspection Management
- Quality Management Systems
- Quality Assurance
- GxP Experience
- Good Manufacturing Practices (cGMP)
- People Management
- Quality Compliance
- Drug Development
- Research
- Technological Expertise
- Complaints Management
- Good Laboratory Practice (GLP) Analytics
- Incident Management
- Deviation Management
- Patient Safety
- Pharmacovigilance
- English proficiency
Aufgaben
- Provide quality assurance and compliance oversight
- Drive quality management systems and initiatives
- Ensure compliance with health authority regulations
- Role model good quality behaviors
- Promote a culture of quality
- Develop and support quality plan initiatives
- Provide QA expertise and guidance
- Implement quality risk-based and GxP processes
- Lead and manage a QA organization
- Collaborate with business partners and quality groups
- Translate QA strategy into operational activities
- Support risk-based process implementation
- Address and sustain quality and compliance gaps
- Implement strategic process improvements
- Review procedural updates and training
- Conduct effectiveness checks
- Monitor Quality Plan implementation
- Support inspection readiness activities
- Participate in regulatory inspections
- Manage inspection preparation and follow-up
- Oversee external service providers and IT systems
- Facilitate and follow up on audits and inspections
- Develop and implement corrective and preventive measures
- Escalate deviations and incidents timely
- Conduct robust investigations and root cause analysis
- Implement corrective actions
- Contribute to lessons learned
- Report technical complaints and adverse events within 24 hours
- Distribute marketing samples where applicable
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – fließend
Benefits
Sonstige Vorteile
- Adjustments for applicants with disabilities
- Involvement of local disability representative (BVP)
Abwechslungsreiche Aufgaben
- Advice on suitable positions
Mentoring & Coaching
- Guidance at all stages of the application process
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Novartis Pharmaceutical Manufacturing GmbH
Branche
Pharmaceuticals
Beschreibung
The company aims to reimagine medicine to improve and extend people's lives.
Noch nicht perfekt?
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Global Head QA Operations Aseptics(m/w/x)
Vollzeitnur vor OrtSeniorSchaftenau - Novartis Pharmaceutical Manufacturing GmbH
QA Compliance Expert – Sampling and Manufacturing(m/w/x)
Vollzeitnur vor OrtBerufserfahrenKundlab 64.023,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Validation Lead(m/w/x)
Vollzeitnur vor OrtBerufserfahrenKundlab 60.212,18 / Jahr