Ferrero
Koordinator Health & Safety(m/w/x)
Full-timeOn-siteNot specified
Stadtallendorf
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CSCSL Behring GmbH (DE)
GMP-Koordinator 3(m/w/x)
Schwalmstadt
Full-timeOn-siteExperienced
Nejo AI Summary
Creating and archiving regulatory documents for global plasma therapy projects. Completed 3.5-year Pharmakant training and 4-5 years experience required. Collaboration with international regulatory teams.
Requirements
- Abgeschlossene 3,5 jährige Ausbildung zum Pharmakanten
- Englischkenntnisse auf Level 2
- Zusätzliche betriebliche Spezialausbildung GMP
- 4 – 5 Jahre Berufserfahrung
Tasks
- Create and maintain GMP-relevant documents
- Archive SOPs and production protocols
- Manage documentation for global projects
- Ensure compliance with international regulatory standards
- Monitor departmental documents for GMP conformity
- Initiate corrective actions and monitoring trends
- Report irregularities and organize training sessions
- Coordinate information with Quality Assurance
- Liaise with the global quality unit
- Process deviations and implement resulting measures
Work Experience
- 4 - 5 years
Education
- Vocational certification
Languages
- English – Basic
Tools & Technologies
- GMP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring GmbH (DE) and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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CSCSL Behring GmbH (DE)
GMP-Koordinator 3(m/w/x)
Schwalmstadt
Full-timeOn-siteExperienced
Nejo AI Summary
Creating and archiving regulatory documents for global plasma therapy projects. Completed 3.5-year Pharmakant training and 4-5 years experience required. Collaboration with international regulatory teams.
Requirements
- Abgeschlossene 3,5 jährige Ausbildung zum Pharmakanten
- Englischkenntnisse auf Level 2
- Zusätzliche betriebliche Spezialausbildung GMP
- 4 – 5 Jahre Berufserfahrung
Tasks
- Create and maintain GMP-relevant documents
- Archive SOPs and production protocols
- Manage documentation for global projects
- Ensure compliance with international regulatory standards
- Monitor departmental documents for GMP conformity
- Initiate corrective actions and monitoring trends
- Report irregularities and organize training sessions
- Coordinate information with Quality Assurance
- Liaise with the global quality unit
- Process deviations and implement resulting measures
Work Experience
- 4 - 5 years
Education
- Vocational certification
Languages
- English – Basic
Tools & Technologies
- GMP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring GmbH (DE) and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
CSL Behring GmbH (DE)
Industry
Pharmaceuticals
Description
Das Unternehmen betreibt eines der weltweit größten Plasma-Entnahme-Netzwerke und stellt lebensrettende Therapien her.
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