Quality Assurance

Located in Holly Hill, FL

Salary: $18-$20

Pay: $18.00 - $20.00 per hour

Job description:

Position Summary
The In-Process QA Inspector is responsible for auditing, enforcing, and maintaining control of in-process quality activities during manufacturing, filling, and packaging operations. This role works cross-functionally with Production, Quality, Warehouse, and Laboratory teams to ensure products and components meet established specifications, documentation requirements, and cGMP expectations. The Inspector identifies deviations in real time, supports timely corrective actions, and recommends process improvements that enhance efficiency and ensure customer and regulatory requirements are consistently met.

Essential Duties & Responsibilities

• Perform in-process line checks, inspections, and verifications per procedures, batch records, and work instructions.
• Confirm correct component usage, packaging configuration, and line setup (e.g., labels, coding, inserts, lot/expiry, counts).
• Document inspection results clearly and accurately in real time, maintaining complete and compliant records.
• Immediately notify supervision and QA leadership of deviations, defects, or out-of-specification conditions; assist with investigations as needed.
• Print, review, and apply component and product status labels/tags in accordance with procedures.
• Collect samples for laboratory testing, retain samples, stability samples, and special requests; prepare and package samples as required.
• Verify labels, UPC/barcode stickers, and printed information for accuracy and legibility throughout the run.
• Support rework activities by communicating requirements and confirming that disposition instructions are followed.
• Operate and use approved inspection and testing tools/equipment properly (e.g., scales, calipers, torque devices, vision systems) as applicable.
• Follow cGMP, safety, and site rules at all times; maintain a clean and organized work area.
• Maintain control and integrity of quality records, including ensuring entries are complete, legible, attributable, and compliant with documentation practices.
• Participate in special projects and other duties as assigned.

We are ideally looking for candidates with:

• 2–5 years of QA inspection experience in cosmetics, OTC, pharmaceutical, or similar regulated industries
• Strong understanding of cGMP and Good Documentation Practices (GDP)
• Experience with incoming inspection, material release, and supplier quality activities
• Strong attention to detail and ability to work cross-functionally
• Ability to work independently and within a team

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