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QA Supervisor (2nd Shift)

  • QA Supervisor (2nd Shift) job type Posted on: Nov 02, 2026
  • QA Supervisor (2nd Shift) experience level Imagine Staffing Technology
  • QA Supervisor (2nd Shift) employment type Lancaster, South Carolina
  • QA Supervisor (2nd Shift) employment type Onsite
  • QA Supervisor (2nd Shift) salary Full-time
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Job Title :

QA Supervisor (2nd Shift)

Job Type :

Full-Time

Job Location :

Lancaster South Carolina United States

Remote :

No

Jobcon Logo Job Description :

View Full Description

Job Description

Job Description
Job Title: Quality Assurance Supervisor – 2nd Shift
Location: Lancaster, SC
Pay Range: $85,000 - $100,000 base salary; eligible for up to 15% annual bonus (not guaranteed)
Work Type: Full-Time
Work Model: Onsite
Work Schedule: Monday – Friday, 3:15pm – 11:30pm (initial training on 1st shift)
Recruiter Contact: Sean Pebbles | spebbles@imaginegroup.com 
 
Nature & Scope:
Positional Overview
The Imagine Group is recruiting for a 2nd Shift Quality Assurance Supervisor on behalf of our client, an FDA-regulated manufacturer of nutritional supplement products committed to product quality, regulatory compliance, and continuous improvement.
Reporting to the Quality Assurance Assistant Manager, this supervisor leads Quality Assurance Inspectors, Label Issuance personnel, and Team Leads. The role oversees daily QA operations, production monitoring, quality systems, and the consistent application of current Good Manufacturing Practices (cGMP). The successful candidate will combine hands-on quality expertise with strong people leadership, accountability, conflict resolution, and a continuous-improvement mindset.
 
Role & Responsibility:
Tasks That Will Lead to Your Success:
  • Supervise and develop QA Inspectors, Label Issuance staff, and Team Leads; provide coaching, performance accountability, conflict resolution, and consistent policy enforcement.
  • Oversee QA inspection activities, production-process monitoring, and label cage operations and personnel.
  • Review and approve protocols; review SOPs, processes, batch records, and procedures, and update documentation to improve consistency and compliance.
  • Partner with Production Supervisors to resolve manufacturing and quality issues, and collaborate with Production, New Product Development, and other departments on quality-system activities.
  • Monitor environmental-condition records, respond to excursions, and review pest-control, calibration, and related quality records.
  • Investigate deviations and nonconformances; assess potential effects on product quality, safety, and purity; prepare and close NCRs and document corrective actions.
  • Ensure compliance with applicable cGMP requirements, FDA regulations, industry standards, and company policies; support product quality and regulatory readiness.
  • Develop and implement processes that strengthen compliance, operational consistency, and continuous improvement, including Lean manufacturing practices where applicable.
  • Enforce safe work practices, identify and correct unsafe conditions, train employees on hazard recognition, and follow up on corrective measures.
  • Coordinate incident response and reporting with EHS and appropriate response teams; support incident investigations, including 5-Why root-cause analysis and corrective actions.
  • Communicate effectively across shifts and departments; periodically adjust shift hours to support personnel on other shifts.
  • Perform additional duties as assigned.
 
Skills & Experience
Qualifications That Will Help You Thrive
  • High school diploma required; an Associate or Bachelor’s degree, preferably in a science-related field, is preferred.
  • 4–5 years of experience in an FDA-regulated manufacturing or production environment, including at least 3 years in Quality Assurance or Quality Control.
  • Experience in nutritional supplements and/or pharmaceutical manufacturing.
  • Strong working knowledge of cGMP, SOPs, batch records, deviations, nonconformances, and quality documentation.
  • Experience with ISO standards, dietary supplements, and Lean manufacturing practices is desirable.
  • Prior FDA or equivalent regulatory inspection experience is highly preferred.
  • Demonstrated supervisory leadership, including difficult employee conversations, performance accountability, conflict resolution, and policy compliance.
  • Strong cross-functional communication skills and a commitment to continuous improvement.
Ability to work the stated second-shift schedule, train initially on first shift, and periodically support other shifts.
 
Additional Position Information
  • Eligible for relocation support, which may include up to 45 days of furnished temporary housing, a $5,000 relocation stipend, paid transportation of personal goods, and paid area-exploration visits.
  • This role may involve exposure to raw materials or finished goods containing allergens or animal-derived ingredients, including milk, soy, shellfish, pork, poultry, fish, eggs, peanuts, tree nuts, wheat, and sesame.
  • Employer sponsorship is not available now or in the future.
 

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Jobcon Logo Position Details

Posted:

Nov 02, 2026

Reference Number:

dddb00e8

Employment:

Full-time

City:

Lancaster

Job Origin:

ziprecruiter

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Job Description

Job Description
Job Title: Quality Assurance Supervisor – 2nd Shift
Location: Lancaster, SC
Pay Range: $85,000 - $100,000 base salary; eligible for up to 15% annual bonus (not guaranteed)
Work Type: Full-Time
Work Model: Onsite
Work Schedule: Monday – Friday, 3:15pm – 11:30pm (initial training on 1st shift)
Recruiter Contact: Sean Pebbles | spebbles@imaginegroup.com 
 
Nature & Scope:
Positional Overview
The Imagine Group is recruiting for a 2nd Shift Quality Assurance Supervisor on behalf of our client, an FDA-regulated manufacturer of nutritional supplement products committed to product quality, regulatory compliance, and continuous improvement.
Reporting to the Quality Assurance Assistant Manager, this supervisor leads Quality Assurance Inspectors, Label Issuance personnel, and Team Leads. The role oversees daily QA operations, production monitoring, quality systems, and the consistent application of current Good Manufacturing Practices (cGMP). The successful candidate will combine hands-on quality expertise with strong people leadership, accountability, conflict resolution, and a continuous-improvement mindset.
 
Role & Responsibility:
Tasks That Will Lead to Your Success:
  • Supervise and develop QA Inspectors, Label Issuance staff, and Team Leads; provide coaching, performance accountability, conflict resolution, and consistent policy enforcement.
  • Oversee QA inspection activities, production-process monitoring, and label cage operations and personnel.
  • Review and approve protocols; review SOPs, processes, batch records, and procedures, and update documentation to improve consistency and compliance.
  • Partner with Production Supervisors to resolve manufacturing and quality issues, and collaborate with Production, New Product Development, and other departments on quality-system activities.
  • Monitor environmental-condition records, respond to excursions, and review pest-control, calibration, and related quality records.
  • Investigate deviations and nonconformances; assess potential effects on product quality, safety, and purity; prepare and close NCRs and document corrective actions.
  • Ensure compliance with applicable cGMP requirements, FDA regulations, industry standards, and company policies; support product quality and regulatory readiness.
  • Develop and implement processes that strengthen compliance, operational consistency, and continuous improvement, including Lean manufacturing practices where applicable.
  • Enforce safe work practices, identify and correct unsafe conditions, train employees on hazard recognition, and follow up on corrective measures.
  • Coordinate incident response and reporting with EHS and appropriate response teams; support incident investigations, including 5-Why root-cause analysis and corrective actions.
  • Communicate effectively across shifts and departments; periodically adjust shift hours to support personnel on other shifts.
  • Perform additional duties as assigned.
 
Skills & Experience
Qualifications That Will Help You Thrive
  • High school diploma required; an Associate or Bachelor’s degree, preferably in a science-related field, is preferred.
  • 4–5 years of experience in an FDA-regulated manufacturing or production environment, including at least 3 years in Quality Assurance or Quality Control.
  • Experience in nutritional supplements and/or pharmaceutical manufacturing.
  • Strong working knowledge of cGMP, SOPs, batch records, deviations, nonconformances, and quality documentation.
  • Experience with ISO standards, dietary supplements, and Lean manufacturing practices is desirable.
  • Prior FDA or equivalent regulatory inspection experience is highly preferred.
  • Demonstrated supervisory leadership, including difficult employee conversations, performance accountability, conflict resolution, and policy compliance.
  • Strong cross-functional communication skills and a commitment to continuous improvement.
Ability to work the stated second-shift schedule, train initially on first shift, and periodically support other shifts.
 
Additional Position Information
  • Eligible for relocation support, which may include up to 45 days of furnished temporary housing, a $5,000 relocation stipend, paid transportation of personal goods, and paid area-exploration visits.
  • This role may involve exposure to raw materials or finished goods containing allergens or animal-derived ingredients, including milk, soy, shellfish, pork, poultry, fish, eggs, peanuts, tree nuts, wheat, and sesame.
  • Employer sponsorship is not available now or in the future.
 

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