Actalent
Location
Santa Ana, CA | United States
Job description
Description:
In need of quality assurance technicians that can come in and help with their QA functions. Will be held responsible for: Reviewing and editing batch records Assisting in Document Change Control and reviewing history records for compliance. Working with Non conformances, discrepancies and dispositions. Assist with investigations for Environmental Monitoring- surface sampling, air sampling, etc. Perform lab work as needed within microbiology and chemistry Perform OS investigations Perform work within quality systems as needed. Examples include supplier management, internal audits, non conformances, risk analysis. Assist with Handling Customer Complaints, support regulatory audits Help with following up with office and lab personnel on documentation. Skills: Gmp, Quality assurance, batch record review, Capa, Audit, non conforming Top Skills Details: Gmp,Quality assurance Additional Skills & Qualifications: Education: Bachelor of Science degree in related field or comparable additional experience. Associates okay with 2 years of FDA quality experience, Bachelors at least 1 year. Pharmaceutical experience preferred FDA/cGMP Experience - 1 year Experience with Microsoft office suite Master control experience is preferred. Experience Level: Entry Level About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Job tags
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