Gmp Auditor Jobs
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TN Switzerland-Basel
global risk-based audit strategy
• Plan, lead, conduct, document, and follow-up of assigned GMP/GDP audits as Lead Auditor
• Manage Global, Regional, and Affiliate internal audits/self-inspections
• Manage external audits of CMOs, CLOs, contract service...
gloor&lang AG-Basel
functional quality improvement initiative focused on streamlining change control handling in regulatory dossiers and release processes.
• Ensure compliance with GMP regulations and pharmaceutical quality standards.
• Provide project management support...
appcast.io -
TN Switzerland-Liesberg
durch Auftragsherstellung und Auslizenzierung zu beliefern.
Die Position
Die Rolle
Diese Position ist verantwortlich für alle GMP- und qualitätsrelevante Themen sowie für das Trainingskonzept innerhalb der Bulk Produktion.
Deine Chancen
• Koordination und Durchführung...
Maropack AG-Zell (ZH)
Auditor
• Management und Bearbeitung von Abweichungen, Reklamationen und Änderungen(Change Control) sowie CAPA Massnahmen
• Durchführung des Batch Record Reviews
• Unterstützung anderer Bereiche in Fragen der GMP-Compliance
• Durchführung...
gloor&lang AG-Basel
testing (to confirm correct amino acid sequence) and impurity profiling.
• Ensure that all testing and controls at the CMO are performed under GMP-compliant conditions.
• Participate in batch record review and deviation management, including the evaluation...
yellowshark-Wald
an einer technischen Fachhochschule, idealerweise mit Schwerpunkt in Fertigungstechnik oder Kunststofftechnik.
• Ausbildung als interner und externer Auditor
• Branchenerfahrung in der Medizin-, Produktions- oder Kunststofftechnik in einem internationalen Umfeld...
CK Group-Bern
electrical installation plans etc.).
• Ausarbeiten und durchführen von Anpassungen an CAD Systemen.
• Data cloud management (Meridian).
• Projekt und Audit support.
• 3D scan data management.
• SAP Stammdaten implementierung (FLOCS). Pf lege von SAP...
yellowshark-Wald
Studium an einer technischen Fachhochschule, idealerweise mit Schwerpunkt in Fertigungstechnik oder Kunststofftechnik.
• Ausbildung als interner und externer Auditor
• Branchenerfahrung in der Medizin-, Produktions- oder Kunststofftechnik...
Lonza Biologics Porriño SLU-Visp
life sciences?
Key responsibilities:
1. Responsible for project-specific QA Operation work during commissioning/qualification in IBEX
2. Assess and manage tasks that would impact Quality operation during GMP manufacturing
3. Plan for future activities...
appcast.io -
Randstad-Bulle
laboratories and Manufacturing. This includesperforming QA oversight, reviewing audit trails, approvingCSV/Qualification documents for equipment (e.g., HPLC, GC, MES),and defining critical data flows to maintain QA integrity. You willalso support KPI...
Lonza Biologics Porriño SLU-Schweiz
life sciences?
Key responsibilities:
• Responsible for project-specific QA Operation work during commissioning/qualification in IBEX
• Assess and manage tasks that would impact Quality operation during GMP manufacturing
• Plan for future activities...
appcast.io -
gloor&lang AG-Zurich
Audit Management - Freigaben - GMP/GDP Lizenzen
Unser Kunde ist ein renommiertes Schweizer Pharmaunternehmen mit langjähriger Tradition und hoher Innovationskraft. Entwicklung, Herstellung und den Vertrieb hochwertiger pharmazeutischer Produkte...
handwerker-Basel
initiative focused on streamlining change control handling in regulatory dossiers and release processes.
• Ensure compliance with GMP regulations and pharmaceutical quality standards.
• Provide project management support, including planning, scheduling...
appcast.io -
gloor & lang Pharma and Biotech Recruiting-Basel
initiative focused on streamlining change control handling in regulatory dossiers and release processes.
• Ensure compliance with GMP regulations and pharmaceutical quality standards.
• Provide project management support, including planning, scheduling...
Randstad (Schweiz) AG-Bulle
laboratories and Manufacturing. This includes performing QA oversight, reviewing audit trails, approving CSV/Qualification documents for equipment (e.g., HPLC, GC, MES), and defining critical data flows to maintain QA integrity. You will also support KPI...
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