Lonza
Associate Director, QA Logistics Functional Lead(m/w/x)
Vollzeitnur vor OrtSenior
Visp
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QA oversight for facility operations and utility systems at a global pharmaceutical manufacturer. Strong GMP-regulated manufacturing and QA leadership experience required. Broad QA topic leadership scope, agile career path.
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Anforderungen
- Academic degree in Life Sciences, Engineering, Pharmaceutical Sciences, Biotechnology, Quality, or relevant discipline
- Significant GMP-regulated manufacturing experience (pharma/biotech)
- Strong QA experience in leading technical/operational topics
- Influencing cross-functional stakeholders
- Driving risk-based decisions without direct line management
- Strong knowledge of GMP requirements and quality systems
- Knowledge of deviations, CAPAs, change controls, risk management
- Knowledge of inspections and audits
- Experience with utilities, infrastructure, pest control, facility readiness
- Experience with engineering, construction, or project handover
- Good understanding of contamination prevention principles
- Good understanding of cleanroom operations and qualified utilities
- Good understanding of GMP facility interfaces and pest control
- Good understanding of inspection readiness
- Ability to translate complex technical/operational/GMP topics
- Ability to provide clear, risk-based decisions and pragmatic quality guidance
- Fluency in English
Aufgaben
- Support QA for facility operations and pest control
- Provide senior technical direction and risk-based guidance
- Ensure QA oversight for utility systems and facility interfaces
- Prevent microbial contamination and cross-contamination
- Maintain GMP compliance and inspection readiness
- Own QA governance for facility operations and pest control
- Review and approve deviations and changes
- Conduct GMP document reviews and approvals
- Oversee CAPA and trend reviews
- Perform quality risk assessments
- Act as QA subject matter expert during audits and inspections
- Provide quality oversight for new projects and facility changes
- Ensure utility standards and infrastructure readiness
- Manage construction segregation and cleanroom interfaces
- Facilitate handover into routine operations
- Collaborate with QA Operations, QC, Hygiene, Engineering, Facilities, Utilities Operations, Manufacturing, Regulatory, Global Quality Engineering, and Global Engineering
- Drive continuous improvement of quality systems
- Enhance inspection readiness and compliance standards
- Promote practical GMP execution
Berufserfahrung
ca. 4 - 6 Jahre
Ausbildung
Bachelor-Abschluss
Sprachen
Englisch – fließend
Deutsch – Grundkenntnisse
Benefits
Lockere Unternehmenskultur
- Inclusive, dynamic, and passionate team
- Dynamic work culture
Sinnstiftende Arbeit
- Broad and high-impact QA topic leadership scope
- Inclusive and ethical workplace
Karriere- und Weiterentwicklung
- Agile career
Boni & Prämien
- Compensation programs that recognize high performance
Mitarbeiterrabatte
- Lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens Lonza erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Zur Originalanzeige bei LonzaÜber das Unternehmen
LO
PharmaceuticalsVisp
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
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