Quality Specialist(3rd Shift)

Ajulia Executive Search; Rock Hill (SC); On-site; USD 42,000 - 66,000; Full time

Job summary

Ajulia Executive Search seeks a Quality Specialist to support manufacturing and packaging on the production floor in Rock Hill, SC. The role emphasizes daily quality review, document accuracy, and adherence to cGMP and company standards.

You will perform in-process inspections, assist with deviations, review batch records, and collaborate with QA, QC, safety, and supply chain teams to maintain compliance and timely reporting.

Qualifications

• 2+ years of experience in a regulated environment (pharmaceutical, food, or dietary supplements preferred).
• Auditing and troubleshooting experience is a plus.
• Strong communication skills and ability to work in a team environment.

Responsibilities

• Support production by performing in-process inspections, room clearances, and equipment/area releases.
• Review documentation for accuracy during manufacturing and packaging.
• Assist with deviation investigations and identify errors in batch records.
• Issue labels and printed materials per production schedule.
• Monitor environmental systems and pest control records.
• Submit end-of-day reports summarizing activities and issues.
• Communicate effectively with production, QA, QC, safety, and supply chain teams.
• Stay current on SOPs, safety procedures, and cGMP training.

Skills

In-process inspections

cGMP compliance

Documentation review

Teamwork

Quality assurance

Job description

The Quality Specialist provides daily quality support during manufacturing and packaging operations. This role reports to Quality Assurance Management and requires a consistent presence on the production floor to review documents, perform inspections, and ensure compliance with cGMP and company standards.

Key Responsibilities

• Support production by performing in-process inspections, room clearances, and equipment/area releases.
• Review documentation for accuracy during manufacturing and packaging.
• Assist with deviation investigations and identify errors in batch records.
• Issue labels and printed materials per production schedule.
• Monitor environmental systems and pest control records.
• Submit end-of-day reports summarizing activities and issues.
• Communicate effectively with production, QA, QC, safety, and supply chain teams.
• Stay current on SOPs, safety procedures, and cGMP training.

Requirements

• 2+ years of experience in a regulated environment (pharmaceutical, food, or dietary supplements preferred).
• Auditing and troubleshooting experience is a plus.
• Strong communication skills and ability to work in a team environment.