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Job Description
QA Specialist at Hydrogen Group QA Specialist at Hydrogen Group in Irvine, California Posted in 1 day ago.
Type:
full-time
Job Description:
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Responsibilities:
Review executed batch records and supporting documentation for completeness, accuracy, and compliance
Support product release activities and ensure adherence to cGMP, GDP, and ALCOA+ principles
Review deviations impacting batch quality and assist with CAPA activities
Maintain quality documentation and support audit and inspection readiness
Identify process improvement opportunities and contribute to quality initiatives ?
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Qualifications:
Bachelor's degree in a scientific discipline preferred (or equivalent experience)
2-4 years of QA experience in a GMP-regulated environment
Experience reviewing batch records and supporting product release activities
Working knowledge of FDA, EMA, and cGMP requirements
Familiarity with quality systems including Deviations, CAPA, Change Control, and Document Control
Strong attention to detail, organizational skills, and documentation practices ?
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Ideal Candidate:
? Experience in pharmaceutical, biotechnology, manufacturing, or other regulated industries ? Strong understanding of quality systems and compliance requirements ? Ability to work independently and manage priorities effectively ? Commitment to quality, integrity, and continuous improvement