Pharmaceutical QA Inspector

Not Ready Important Notice About the Application Process This position offers use of our AI screening tool as part of the initial candidate review. While completing the AI screening is optional, please note: Candidates who complete the AI screening are reviewed first—daily. We strongly encourage you to complete it promptly to ensure early consideration (first come, first served). Expect to receive a prompt from our AI screener shortly after applying. The AI screener helps us streamline the Candidate intake process, but rest assured— you'll still work directly with a Masis recruiter throughout the rest of your hiring journey. QA Line Inspector•

Pharmaceutical Packaging Shift:

2nd Shift (3:00 PM•11:30 PM)

Duration:

3-month contract (possible extension or direct hire)

Pay Rate:

$22•25/hour + Overtime Job Summary We are seeking a detail-oriented QA Line Inspector to support pharmaceutical packaging operations in a pharmaceutical manufacturing environment. This role ensures packaging activities meet cGMP requirements and internal quality standards through line inspections, documentation, and batch record control. Key Responsibilities Provide QA support and oversight on the packaging line. Perform line clearance and start-up inspections and approve packaging run start. Issue and maintain packaging batch records and related documentation. Verify packaging materials/components match the approved Bill of Materials (BOM). Document in-process inspections and retain required samples. Review completed batch records for accuracy and compliance. Label and control finished goods leaving the packaging area (Released, Quarantined, etc.). Ensure proper disposition and destruction of unused packaging components (labels, cartons, inserts, etc.). Communicate quality issues impacting line clearance, setup, or inspection results. Support packaging teams with quality-related questions and concerns. Work overtime or weekends as needed. Qualifications 3+ years of QA experience in a pharmaceutical, biotech, or regulated manufacturing environment (required). Knowledge of cGMP regulations and quality standards. Strong attention to detail with batch record documentation. Good communication and organizational skills. Ability to work effectively with cross-functional teams. Proficient in Microsoft Office (Word, Excel, Outlook). SAP and/or TrackWise experience preferred. Strong critical thinking and problem-solving skills. #MPG1

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