QA Inspector
Quality Assurance Inspector - 2nd & 3rd Shift
Full‑Time | On‑Site - Lancaster, SC| $49,920-$53,040 Annualized (Depending on Shift)
Relocation considered for strong candidates
A growing FDA‑regulated manufacturing company in the Southeast is hiring multiple Quality Assurance Inspectors to support expanding manufacturing and packaging operations. These are fully on‑site roles with openings on 2nd shift and 3rd shift, and brief training on 1st shift may be required.
This role is well suited for someone who wants to develop within a structured Quality organization and enjoys hands‑on involvement with daily operations.
About the Role
The QA Inspector provides real‑time quality oversight on the production floor, ensuring all manufacturing and packaging activities comply with cGMP requirements and internal quality standards. Responsibilities include in‑process inspections, room and equipment clearances, batch record review, label issuance, and supporting deviation investigations. This position requires a strong physical presence in manufacturing areas and regular interaction with operations teams.
Key Responsibilities
- Maintain QA presence on manufacturing and packaging floors
- Conduct in‑process inspections, room clearances, and equipment/area releases
- Review batch records and identify documentation errors or gaps
- Issue labels and printed materials per production schedules
- Support deviation investigations and basic root cause analysis
- Review environmental monitoring and pest control documentation
- Support QA Hold processes
- Submit end‑of‑shift reports summarizing quality events and actions
- Maintain current training on SOPs, safety procedures, and cGMPs
- Communicate effectively across operations, QC, safety, supply chain, and product development
Minimum Qualifications
- High School Diploma or equivalent
- At least two years working in a regulated manufacturing environment (pharma, dietary supplements, food, or similar)
- Experience working on the production floor
- Strong attention to detail and comfort reviewing documents
- Ability to wear PPE and lift up to 50 lbs
- Ability to pass a background check, drug screen, and reading comprehension test
- U.S. work authorization (no sponsorship)
Compensation
Annualized Range: $49,920 - $53,040
- $24/hr base
- $1.00/hr differential for 2nd shift
- $1.50/hr differential for 3rd shift
- Full benefits package including medical, dental, vision, 401k, tuition assistance, childcare support, and disability insurance
Shift Schedule
- 2nd Shift: Monday-Thursday 3:15pm-11:30pm, Friday 3:15pm-10:15pm
- 3rd Shift: Sunday-Thursday 11:15pm-7:15am
- Temporary 1st shift training may be required
Why This Role Is Attractive
This position offers consistent work, long‑term stability, strong cross‑functional exposure, and clear growth pathways into roles such as QA Specialist, Quality Systems, Documentation, and other areas of Quality. It is a strong fit for candidates who want to build a career in regulated manufacturing and gain daily experience in GMP compliance.
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