Responsibilities:
- You ,aintain Quality Assurance Systems/affiliate quality management system to ensure compliance with company standards and regulatory guidelines
- You manage staff and GMP systems for ensuring quality of incoming materials /timely release of CSL products to the market
- You support investigations/affiliate recalls and reporting of product technical complaints and ensures remedial actions are implemented
- You collaborate across departments to resolve customer inquiries and possible temperature storage concerns
- You establish and maintain GXP training and site quality policies, SOPs and work instructions
- Together with Global Supplier Quality, supports management of Quality Agreements
Qualifications:
- Bachelor's degree in a relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry)
- 5+ years' GMP experience in pharmaceutical/biotech/or other regulated industry
- Experience within a global matrix organization
- Knowledge of current Good Manufacturing Practices (cGMP) principles
- Knowledge of regulatory requirements
Our Benefits
We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.
About CSL Behring
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.
We want CSL to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.
Do work that matters at CSL Behring!
More Information
Application Details
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Organization Details
1095 CSL Behring AG (CH)
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