QA Specialist (Biotech)
- Expired: over a month ago. Applications are no longer accepted.
Your main responsibilities as a QA Specialist I:
· Disposition raw materials globally for company manufacturing network
· Review material related documentation and ensure resolution of issues to release material
· Manage company’s Quality Systems for Global Raw Materials and Reagents group
· Provide quality oversight for the QC lab for raw material testing
· Execute Quality walk through for QC Lab for raw material testing
What we are looking for in a QA Specialist I:
· Master’s Degree and 5+ years’ experience in cGMP regulations, quality systems and regulatory requirements OR Bachelor’s Degree and 7+ years’ experience in cGMP
regulations, quality systems and regulatory requirements OR High School Degree
and 11+ years’ experience in cGMP regulations, quality systems and regulatory
requirements
· Degree in the biological sciences or related field
· Direct management/leadership experience in a pharmaceutical or biologics operation.
· Experience in identifying, writing, evaluating and closing CAPAs.
· Experience with conducting and managing internal and external audits.
R&D Partners
Address
Santa Monica, CAIndustry
Technology
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