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Group Senior Analytical Specialist - QC Method Compliance(m/w/x)
Supporting analytical method validation and transfer for plasma-derived protein products. Pharmaceutical QC experience and GMP knowledge required. Company restaurant and meal subsidy.
Requirements
- Degree in Life Sciences, Chemistry, Pharmacy, or related field
- Experience in pharmaceutical industry Quality Control
- Good understanding of GMP requirements and analytical data evaluation
- Strong organizational, communication, and project management skills
- Confident handling of MS Office and data/documentation systems
- Fluent English skills
Tasks
- Support analytical method validation
- Collaborate on method transfer activities
- Conduct method comparison activities
- Coordinate validation planning
- Document validation activities
- Evaluate validation data
- Report validation results
- Prepare validation documentation
- Review validation documents
- Maintain Master Methods of Analysis
- Update product specifications
- Troubleshoot with global QC stakeholders
- Investigate issues with QC stakeholders
- Manage QC-related databases
- Maintain corporate document management systems
- Coordinate reference material calibration
- Document calibration activities
- Verify reference material stability
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- MS Office
Benefits
Free or Subsidized Food
- Company restaurant
- Meal subsidy
Learning & Development
- Training and further education
Healthcare & Fitness
- Health promotion
Parking & Commuter Benefits
- Parking spaces
- Good public transport connections
Team Events
- Company and team events
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Group Senior Analytical Specialist - QC Method Compliance(m/w/x)
Supporting analytical method validation and transfer for plasma-derived protein products. Pharmaceutical QC experience and GMP knowledge required. Company restaurant and meal subsidy.
Requirements
- Degree in Life Sciences, Chemistry, Pharmacy, or related field
- Experience in pharmaceutical industry Quality Control
- Good understanding of GMP requirements and analytical data evaluation
- Strong organizational, communication, and project management skills
- Confident handling of MS Office and data/documentation systems
- Fluent English skills
Tasks
- Support analytical method validation
- Collaborate on method transfer activities
- Conduct method comparison activities
- Coordinate validation planning
- Document validation activities
- Evaluate validation data
- Report validation results
- Prepare validation documentation
- Review validation documents
- Maintain Master Methods of Analysis
- Update product specifications
- Troubleshoot with global QC stakeholders
- Investigate issues with QC stakeholders
- Manage QC-related databases
- Maintain corporate document management systems
- Coordinate reference material calibration
- Document calibration activities
- Verify reference material stability
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- MS Office
Benefits
Free or Subsidized Food
- Company restaurant
- Meal subsidy
Learning & Development
- Training and further education
Healthcare & Fitness
- Health promotion
Parking & Commuter Benefits
- Parking spaces
- Good public transport connections
Team Events
- Company and team events
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Octapharma
Industry
Pharmaceuticals
Description
Das Unternehmen ist eines der weltweit größten, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt.
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