Quality Assurance Inspector II - 2nd Shift

Role: QA Inspector I responsible for sampling, inspecting, testing, and ensuring compliance of raw materials, packaging components, returned goods, and manufacturing processes in a biopharma setting. Primary objectives include maintaining product quality, verifying GMP adherence, and supporting batch release activities. Responsibilities encompass detailed inspection and testing of incoming materials, packaging components, and finished products; documentation of sampling and testing activities; monitoring environmental conditions; reviewing batch records and equipment functionality; managing labeling components and quarantine areas; and performing environmental monitoring and disposition of rejected materials. Requirements: High School diploma or GED; at least 2 years of QA or related experience; strong attention to detail, basic math skills, and record-keeping abilities. Certifications include OSHA-compliant Respirator Fit Test. Preferred qualifications are not specified. High-value specifics: this position supports pharmaceutical manufacturing, likely involving sterile or non-sterile drug products, with responsibilities aligned to GMP standards, quality control, batch record review, and environmental monitoring. The role operates on 2nd shift (3:30 pm – 12:00 am, Monday to Friday). No specific therapeutic areas or modalities are indicated, but the focus on drug manufacturing and GMP compliance is central.