Quality Assurance Inspector; Manufacturing

Job Title and Location

Quality Assurance Inspector (Manufacturing) | Direct Hire Opportunity

Location: Lancaster, SC

Pay Rate: $22.00 - $24.00 per hour | Multiple Shifts Available

Shifts
:

2nd Shift: 3:15 PM – 11:30 PM, Monday–Thursday; 3:15 PM – 10:15 PM on Friday

3rd Shift: 11:15 PM – 7:15 AM, Sunday–Thursday

Staffmark is hiring a Quality Assurance Inspector (Manufacturing) to support production quality, documentation accuracy, and compliance standards in a fast-paced manufacturing environment. The role focuses on maintaining high-quality products and collaborating with the production team.

• Provide quality assurance support throughout daily manufacturing and packaging operations.
• Maintain a consistent presence on the production floor to support quality standards and production activities.
• Perform in-process inspections to verify products meet quality, safety, and compliance requirements.
• Review production documentation, batch records, and manufacturing paperwork for accuracy and completeness.
• Conduct room clearances and release cleaned equipment, rooms, and production areas.
• Issue labels and printed production materials according to manufacturing schedules.
• Identify and document minor and major errors, deficiencies, and quality concerns.
• Support investigations related to production deviations and quality issues.
• Review environmental monitoring and pest control documentation.
• Assist with daily operations within the Quality Assurance Hold area.
• Provide input and support for updates to Standard Operating Procedures (SOPs).
• Complete detailed end-of-shift reports outlining activities, issues identified, and actions taken.
• Communicate effectively with Manufacturing, Packaging, Quality Control, Supply Chain, Product Development, Safety, and other departments.
• Follow all cGMP requirements, safety procedures, and company quality standards.
• Perform additional duties as assigned to support business goals.

• High school diploma or GED required.
• A minimum of 2 years of quality assurance experience in pharmaceutical, food, or dietary supplement manufacturing, or another regulated industry is preferred.
• Experience working in a cGMP-regulated environment preferred.
• Auditing, inspection, or troubleshooting experience is a plus.

• A minimum of 2 years of experience in pharmaceutical, food, or dietary supplement manufacturing, or another regulated manufacturing environment is preferred.
• Previous experience in quality assurance, quality control, manufacturing inspection, or production quality is preferred.
• Knowledge of Current Good Manufacturing Practices (cGMP) preferred.
• Experience reviewing batch records, production documentation, and quality paperwork.
• Strong attention to detail with the ability to identify errors, inconsistencies, and quality concerns.
• Experience with audits, investigations, troubleshooting, or corrective actions is a plus.
• Ability to interpret and follow Standard Operating Procedures (SOPs) and written instructions.
• Strong organizational skills with the ability to prioritize daily tasks and meet production goals.
• Effective verbal and written communication skills.
• Ability to work collaboratively with manufacturing, packaging, quality, and support teams.
• Strong computer skills, including Microsoft Office Suite.
• Reliable attendance and dependable work ethic.
• Commitment to maintaining a safe, compliant, and quality-focused workplace.

• Provide quality assurance support throughout daily manufacturing and packaging operations.
• Maintain a consistent presence on the production floor to support quality standards and production activities.
• Perform in-process inspections to verify products meet quality, safety, and compliance requirements.
• Review production documentation, batch records, and manufacturing paperwork for accuracy and completeness.
• Conduct room clearances and release cleaned equipment, rooms, and production areas.
• Issue labels and printed production materials according to manufacturing schedules.
• Assist with identifying and documenting minor and major errors, deficiencies, and quality concerns.
• Support…