QA Line 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. Quality Assurance Line Inspector•2nd

Shift Shift:

2nd Shift (3:00 PM•11:30 PM)

Duration:

3-month contract (possible extension or direct hire)

Pay Rate:

$20•23/hour +

Overtime Job Overview:

Immediate opening for an experience Quality Assurance (QA) Line Inspector to support packaging operations at a pharmaceutical manufacturing site. This is an immediate need for a 3-month contract position with potential extension or direct hire based on business need and performance.

Responsibilities:

Provide QA presence on the packaging line to ensure overall product quality. Perform line clearance and start-up inspections; authorize start of packaging runs. Document all packaging line activities in accordance with established procedures. Issue master batch records and generate Bills of Materials (BOMs) for packaging. Verify that all materials/components used in packaging runs match the approved BOM . Maintain, review, complete, and control packaging batch records to ensure accuracy and compliance. Document in-process inspections and retain required samples. Control and label finished goods leaving the packaging area (Released, Quarantined, etc.). Ensure proper usage, disposition, and destruction of unused packaging components (cartons, labels, inserts, etc.). Communicate any issues affecting packaging line clearance, setup, and inspections. Provide oversight and support to packaging teams regarding quality concerns. Willingness to work overtime and provide coverage as needed, including possible weekend work.

Qualifications:

Associate degree (2-year degree) in a science or technical field preferred . 3+ years of relevant QA experience in a pharmaceutical, biotech, or regulated manufacturing environment

MANDATORY.

Strong understanding of pharmaceutical cGMP requirements, industry standards, and regulations. Excellent verbal and written communication skills. Strong attention to detail and organizational skills, especially related to batch record documentation. Ability to work effectively across departments and with different levels of leadership. Proficiency with Microsoft Office (Outlook, Excel, Word). Experience with systems such as SAP and TrackWise is a plus. Strong critical thinking and problem-solving skills. Physical Requirements This role requires the ability to stand and walk for extended periods, perform repetitive hand motions, and occasionally lift or carry up to 50 lbs. #MPG1

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