What are the responsibilities and job description for the Quality Assurance Technician - 2nd Shift position at Resource Label Group?
Quality Assurance Technician – Job Description
Status: Full-Time / Hourly, Non-Exempt
Supervisor: Quality Assurance Lead Work Schedule: M-F, 5:30 PM – 2:00 AM (fixed start, 8-hour shift)
will work their first 2 weeks on 1st shift for training, then transition to regular 2nd shift schedule
Job Summary
The Quality Assurance Technician is responsible for ensuring compliance with industry Quality standards through meticulous inspection of product at each stage of production, thorough and accurate documentation, and coordinating QA processes at all levels to ensure compliance. This role is documentation-heavy and requires hands-on involvement in quality operations. The ideal candidate has pharmaceutical-specific QA experience and a strong understanding of cGMP-compliant processes.
Responsibilities
Status: Full-Time / Hourly, Non-Exempt
Supervisor: Quality Assurance Lead Work Schedule: M-F, 5:30 PM – 2:00 AM (fixed start, 8-hour shift)
will work their first 2 weeks on 1st shift for training, then transition to regular 2nd shift schedule
Job Summary
The Quality Assurance Technician is responsible for ensuring compliance with industry Quality standards through meticulous inspection of product at each stage of production, thorough and accurate documentation, and coordinating QA processes at all levels to ensure compliance. This role is documentation-heavy and requires hands-on involvement in quality operations. The ideal candidate has pharmaceutical-specific QA experience and a strong understanding of cGMP-compliant processes.
Responsibilities
- Inspects first article, in-process, and final release of product to ensure conformance with regulatory and customer specifications.
- Conduct periodic rounds to all presses, cutting machines, folders, and pack-outs to ensure conformance of product.
- Verifies that cartons of finished products are properly packed and labeled.
- Maintain organized and accurate QA records and documentation of Deviations, CAPAs, NCRs, and Customer Complaints for KPI reporting.
- Performs rub tests and bar code scans when applicable.
- Performs periodic comparator checks of printed products.
- Collaborate with QA Lead to gather information for all investigations, internal and external audits.
- Support the rework or disposition of defective product when necessary, ensuring all actions are thoroughly documented.
- Keep work area clean and organized.
- Adhere strictly to company Standard Operating Procedures (SOP’s) and current Good Manufacturing Practices (cGMP’s).
- Other duties as assigned.
- High School diploma or GED required; with a minimum of one year of experience in quality control, preferably in the printing industry.
- Working knowledge of computer systems.
- Strong attention to detail, organization, and effective communication skills.
- Must have at least a basic understanding of Deviations, CAPAs, SOPs, batch records, and other regulatory documentation.
- Must be able to read a ruler to 1/64”.
- Must be able to sit, stand, stoop, reach, and walk for extended periods.
- Ability to lift up to 50 pounds and use hands and fingers dexterously in continuous and repetitive motions.