You’ll need
Education
✓Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs
✓Bachelor's degree in Nursing or other relevant healthcare profession, or a combination of comparable clinical education and / or experience
Qualifications
✓At least 1 year of experience in toxicology, chemistry, regulation of biologics Experience in reviewing cGMP/GLP related documents (SOP’s, protocols, batch records, technical reports, etc.)
✓Collaborate with stakeholders to conduct compound/product specific risk assessments, as required, for all aspects of the drug development process
✓Must possess technical vocabulary to meet facility needs
✓Ability to listen, collect information, and give instructions in an effort to support, clarify, or resolve problems
✓The ability to draft and review Standard Operating Procedures (SOPs), batch records, and technical reports that are audit-ready and clear
✓Must be able to write clear technical reports in the scientific format
✓Ability to work well under pressure to meet commitments and to remain flexible with a variety of changing demands
✓Ability to work as a member of a team and to assist colleagues as needed
✓Ability to function and work in a diverse work environment
✓Consideration for Work Authorization Sponsorship Must be able to provide proof of work authorization
Benefits
Retirement plan
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About the role
issues of diverse scope and determines solutions. Custom Scope (customizable, will be used in the job posting/advertisement): The Quality Assurance (QA) Specialist will support a Quality Assurance Unit in the School of Medicine, cGMP Facility. The QA Specialist will report administratively to the Manager of Quality Assurance for GMP Operations.