Die KI-Suchmaschine für Jobs
Senior Engineer CSV(m/w/x)
Beschreibung
In this role, you will play a crucial part in shaping the future of the Automation department by ensuring cGMP compliance and maintaining high-quality standards. Daily activities will involve collaborating with various teams, managing inspections, and implementing effective validation strategies.
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Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Adherence to Good Manufacturing Practices (GMP) Safety Standards
- •Proven expertise in CSV
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Assist in deploying and overseeing quality systems for cGMP compliance
- •Ensure a unified approach to systems validation in the Automation department
- •Support Manufacturing Engineering management with CSV activities
- •Maintain validation of cGMP Execution Systems in an inspection-ready state
- •Act as a delegate for internal and external CSV inspections and audits
- •Manage deviations within the Automation department
- •Track GMP trends to implement effective CSV practices
- •Define validation strategies for computerized systems
- •Collaborate with peers in Automation, IT, Quality Management, and Engineering
- •Serve as a liaison between departmental teams and the DI officer
- •Conduct regular DI Surveillance through Gemba Walks and trainings
Sprachen
Englisch – verhandlungssicher
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Senior Engineer CSV(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will play a crucial part in shaping the future of the Automation department by ensuring cGMP compliance and maintaining high-quality standards. Daily activities will involve collaborating with various teams, managing inspections, and implementing effective validation strategies.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Adherence to Good Manufacturing Practices (GMP) Safety Standards
- •Proven expertise in CSV
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Assist in deploying and overseeing quality systems for cGMP compliance
- •Ensure a unified approach to systems validation in the Automation department
- •Support Manufacturing Engineering management with CSV activities
- •Maintain validation of cGMP Execution Systems in an inspection-ready state
- •Act as a delegate for internal and external CSV inspections and audits
- •Manage deviations within the Automation department
- •Track GMP trends to implement effective CSV practices
- •Define validation strategies for computerized systems
- •Collaborate with peers in Automation, IT, Quality Management, and Engineering
- •Serve as a liaison between departmental teams and the DI officer
- •Conduct regular DI Surveillance through Gemba Walks and trainings
Sprachen
Englisch – verhandlungssicher
Über das Unternehmen
CHE-106.649.671 Fisher Clinical Services GmbH
Branche
Other
Beschreibung
The company is dedicated to making the world healthier, cleaner, and safer through scientific research and solutions.
- Thermo Fisher Scientific Inc.
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Vollzeit/Teilzeitnur vor OrtSeniorBülach - Fisher Clinical Services GmbH
USP Manufacturing Team Leader(m/w/x)
Vollzeitnur vor OrtManagementLengnau - Thermo Fisher Scientific Inc.
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