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Group Expert Analytical Specialist - Quality Control(m/w/x)
Developing and validating analytical test methods for human protein products, coordinating method transfers across sites. Experience in GMP environments and statistical analysis required. Global scope in human protein manufacturing.
Requirements
- University degree in natural sciences or equivalent
- Experience in GMP environments and statistical analysis
- Knowledge of Analytical Chemistry, statistics, and GMP
- Advanced MS Office and Excel skills
- Excellent English, interpersonal, and presentation skills
- Problem-solving, time-management, and multitasking skills
Tasks
- Develop and validate analytical test methods
- Ensure compliance with GMP and pharmaceutical standards
- Review method validation protocols and risk assessments
- Troubleshoot and evaluate analytical data
- Coordinate method transfers across different sites
- Establish group-wide analytical standards and controls
- Maintain reference systems and global standards
- Communicate regularly with the test laboratory
- Lead global QC projects across departments
- Perform cross-site comparisons of potency parameters
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- MS Office
- Excel
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 Expert Analytical Specialist - Quality Control(m/w/x)
Developing and validating analytical test methods for human protein products, coordinating method transfers across sites. Experience in GMP environments and statistical analysis required. Global scope in human protein manufacturing.
Requirements
- University degree in natural sciences or equivalent
- Experience in GMP environments and statistical analysis
- Knowledge of Analytical Chemistry, statistics, and GMP
- Advanced MS Office and Excel skills
- Excellent English, interpersonal, and presentation skills
- Problem-solving, time-management, and multitasking skills
Tasks
- Develop and validate analytical test methods
- Ensure compliance with GMP and pharmaceutical standards
- Review method validation protocols and risk assessments
- Troubleshoot and evaluate analytical data
- Coordinate method transfers across different sites
- Establish group-wide analytical standards and controls
- Maintain reference systems and global standards
- Communicate regularly with the test laboratory
- Lead global QC projects across departments
- Perform cross-site comparisons of potency parameters
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- MS Office
- Excel
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
About the Company
Octapharma Pharmazeutika Produktionsges.m.b.H.
Industry
Pharmaceuticals
Description
Octapharma ist eines der weltweit größten Unternehmen, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt.
Not a perfect match?
- Octapharma Pharmazeutika Produktionsges.m.b.H.
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Full-timeOn-siteJuniorWienfrom 4,270.14 / month - Octapharma Pharmazeutika Produktionsges.m.b.H.
Quality Control Coordinator(m/w/x)
Full-timeOn-siteSeniorWienfrom 4,686.11 / month - Octapharma Pharmazeutika Produktionsges.m.b.H.
Group Senior Expert - API Production(m/w/x)
Full-timeOn-siteSeniorWien, Springefrom 4,270.14 / month - Octapharma
Deputy Head QC Projects(m/w/x)
Full-timeTemporary contractOn-siteExperiencedWienfrom 4,686.11 / month - Octapharma
Group Quality LIMS Specialist - International Early Career Program(m/w/x)
Full-timeOn-siteJuniorWienfrom 4,270.14 / month