Dein persönlicher KI-Karriere-Agent
Optimizing CSV strategy for biopharmaceutical therapies, including system evaluation and procedural document implementation. Over 10 years of pharmaceutical quality management and 5 years of CSV experience required. Inclusive and respectful workplace, Equal-Pay certified.
Anforderungen
- Master’s degree in Science, Engineering, or Clinical discipline
- Over 10 years Quality Management experience in pharmaceutical industry
- At least 5 years CSV and qualification experience
- Strong working knowledge of GxP
- Strong working knowledge of 21 CFR Part 11
- Strong working knowledge of EU Annex 11
- Strong working knowledge of GAMP 5
- Strong working knowledge of ICH GCP E6
- Experience in risk-based analysis for AI solutions
- Experience in validation for AI solutions
- Proven experience managing audits
- Proven experience conducting audits
- Strategic thinking
- Risk-based approach application
- Balancing high-level oversight and operational efficiency
- Proven track record leading teams of CSV professionals
- Proven track record developing teams of CSV professionals
- Experience in fast-paced environments
- Deliverables-driven
- Pragmatic
- Thriving in dynamic, fast-paced, matrix environment
- Fluent English
- Fluency in any other European language an asset
Aufgaben
- Lead and optimize CSV strategy for Debiopharm International SA
- Evaluate and design CSV strategy for current and new systems
- Implement CSV strategy in procedural documents
- Contribute to vendor selection and qualification
- Provide proactive quality oversight for GxP critical systems
- Direct CSV approach for project teams
- Supervise creation and approval of deliverables
- Manage test defects and risk mitigation activities
- Oversee computerized system portfolio
- Manage change controls and periodic reviews
- Maintain systems after business go-live
- Advise on CSV regulations and AI projects
- Mentor staff on CSV and CSLC activities
- Manage and develop CSV team
- Ensure high-quality delivery across portfolio initiatives
- Identify areas for process improvement
- Assist with change management
- Support audit planning and CAPA formulation
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – fließend
- other – Grundkenntnisse
Tools & Technologien
- GxP
- 21 CFR Part 11
- EU Annex 11
- GAMP 5
- ICH GCP E6
- AI
Benefits
Lockere Unternehmenskultur
- Inclusive and respectful workplace
Attraktive Vergütung
- Equal-Pay certified
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Optimizing CSV strategy for biopharmaceutical therapies, including system evaluation and procedural document implementation. Over 10 years of pharmaceutical quality management and 5 years of CSV experience required. Inclusive and respectful workplace, Equal-Pay certified.
Anforderungen
- Master’s degree in Science, Engineering, or Clinical discipline
- Over 10 years Quality Management experience in pharmaceutical industry
- At least 5 years CSV and qualification experience
- Strong working knowledge of GxP
- Strong working knowledge of 21 CFR Part 11
- Strong working knowledge of EU Annex 11
- Strong working knowledge of GAMP 5
- Strong working knowledge of ICH GCP E6
- Experience in risk-based analysis for AI solutions
- Experience in validation for AI solutions
- Proven experience managing audits
- Proven experience conducting audits
- Strategic thinking
- Risk-based approach application
- Balancing high-level oversight and operational efficiency
- Proven track record leading teams of CSV professionals
- Proven track record developing teams of CSV professionals
- Experience in fast-paced environments
- Deliverables-driven
- Pragmatic
- Thriving in dynamic, fast-paced, matrix environment
- Fluent English
- Fluency in any other European language an asset
Aufgaben
- Lead and optimize CSV strategy for Debiopharm International SA
- Evaluate and design CSV strategy for current and new systems
- Implement CSV strategy in procedural documents
- Contribute to vendor selection and qualification
- Provide proactive quality oversight for GxP critical systems
- Direct CSV approach for project teams
- Supervise creation and approval of deliverables
- Manage test defects and risk mitigation activities
- Oversee computerized system portfolio
- Manage change controls and periodic reviews
- Maintain systems after business go-live
- Advise on CSV regulations and AI projects
- Mentor staff on CSV and CSLC activities
- Manage and develop CSV team
- Ensure high-quality delivery across portfolio initiatives
- Identify areas for process improvement
- Assist with change management
- Support audit planning and CAPA formulation
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – fließend
- other – Grundkenntnisse
Tools & Technologien
- GxP
- 21 CFR Part 11
- EU Annex 11
- GAMP 5
- ICH GCP E6
- AI
Benefits
Lockere Unternehmenskultur
- Inclusive and respectful workplace
Attraktive Vergütung
- Equal-Pay certified
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Debiopharm
Branche
Pharmaceuticals
Beschreibung
Debiopharm is a privately-owned Swiss biopharmaceutical company committed to research in oncology and infectious diseases to improve patient outcomes and quality of life.
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