Fisher Clinical Services GmbH
Lead QC Technician(m/w/x)
Vollzeitnur vor OrtSenior
Lengnau
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
THThermo Fisher Scientific Inc.
Senior CQV Engineer(m/w/x)
Lengnau
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Preparing, reviewing, and approving validation documents and audit responses for GMP systems. Bachelor's degree in a technical field and 3+ years of pharmaceutical validation experience required. Collaboration with Quality Assurance and System Owners.
Anforderungen
- Bachelor’s degree in Biotechnology, Quality, Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or related field
- Master's degree or Bachelor's degree + 3 years in engineering, preferably in pharmaceutical or chemical process industry
- Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility
- Experience in pharmaceutical industry for qualification & validation
- Experience in multi-cultural work environment
- Excellent verbal and written communication skills in English
- Preferably German or another European language
- Strong understanding of GMP standards and regulatory requirements
- Excellent technical writing skills with attention to detail
- Proficiency in PC applications, including MS Office
- Strong communication and interpersonal skills
- Certification in technical writing or quality management
- Experience with electronic documentation management systems (e.g., Documentum, TrackWise)
Aufgaben
- Prepare, review, and approve production, validation, audit reports, documents, procedures, and rationales
- Evaluate new regulations, changes to existing regulations, and regulatory trends
- Prepare inspections and customer audit responses and reports
- Perform gap analysis to resolve inefficiencies and take appropriate actions
- Define requalification strategy for GMP systems in collaboration with Quality Assurance and System Owners
- Implement requalification strategy, including maintaining the quality system and completing practical activities
- Coordinate execution of activities by external contractors
- Perform requalification and revalidation Work Orders, including routine and non-routine operations
- Document requalification and revalidation activities in forms and OMX following Good Documentation Practices
- Participate in the culture of continuous improvement and development of technologies
- Identify training needs and develop training programs
- Work in a safe and responsible manner to build an injury-free and incident-free workplace
- Participate in calibration activities
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
- Baskisch – Grundkenntnisse
Tools & Technologien
- MS Office
- Documentum
- TrackWise
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Thermo Fisher Scientific Inc. 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.
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THThermo Fisher Scientific Inc.
Senior CQV Engineer(m/w/x)
Lengnau
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Preparing, reviewing, and approving validation documents and audit responses for GMP systems. Bachelor's degree in a technical field and 3+ years of pharmaceutical validation experience required. Collaboration with Quality Assurance and System Owners.
Anforderungen
- Bachelor’s degree in Biotechnology, Quality, Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or related field
- Master's degree or Bachelor's degree + 3 years in engineering, preferably in pharmaceutical or chemical process industry
- Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility
- Experience in pharmaceutical industry for qualification & validation
- Experience in multi-cultural work environment
- Excellent verbal and written communication skills in English
- Preferably German or another European language
- Strong understanding of GMP standards and regulatory requirements
- Excellent technical writing skills with attention to detail
- Proficiency in PC applications, including MS Office
- Strong communication and interpersonal skills
- Certification in technical writing or quality management
- Experience with electronic documentation management systems (e.g., Documentum, TrackWise)
Aufgaben
- Prepare, review, and approve production, validation, audit reports, documents, procedures, and rationales
- Evaluate new regulations, changes to existing regulations, and regulatory trends
- Prepare inspections and customer audit responses and reports
- Perform gap analysis to resolve inefficiencies and take appropriate actions
- Define requalification strategy for GMP systems in collaboration with Quality Assurance and System Owners
- Implement requalification strategy, including maintaining the quality system and completing practical activities
- Coordinate execution of activities by external contractors
- Perform requalification and revalidation Work Orders, including routine and non-routine operations
- Document requalification and revalidation activities in forms and OMX following Good Documentation Practices
- Participate in the culture of continuous improvement and development of technologies
- Identify training needs and develop training programs
- Work in a safe and responsible manner to build an injury-free and incident-free workplace
- Participate in calibration activities
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
- Baskisch – Grundkenntnisse
Tools & Technologien
- MS Office
- Documentum
- TrackWise
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Thermo Fisher Scientific Inc. 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.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Thermo Fisher Scientific Inc.
Branche
Pharmaceuticals
Beschreibung
The company is a world leader in serving science, enabling customers to make the world healthier, cleaner, and safer.
Noch nicht perfekt?
- Fisher Clinical Services GmbH
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Vollzeitnur vor OrtBerufserfahrenWettingen - HITACHI ENERGY LTD
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Vollzeitnur vor OrtSeniorLenzburg