Quality Assurance Supervisor 3rd shift
Listed on 2026-08-04
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Production QC/QA, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Quality Assurance Supervisor 3rd shift (PR/603919) Lancaster, South Carolina
Salary: USD
75000 - USD
85000 per year
Quality Assurance Supervisor3 rd shift
Hours:Sunday – Thursday 11:15pm– 7:15am(Training would take place on1 st )
Position Overview
We are seeking a Quality Assurance Supervisor to oversee quality operations on our 3rd shift manufacturing team. This individual will play a critical role in ensuring compliance with FDA regulations, internal quality systems, and manufacturing standards while driving continuous improvement initiatives across the organization.
The ideal candidate is a hands‑on quality professional with strong leadership capabilities who thrives in a fast‑paced manufacturing environment. This role requires someone who can effectively manage quality processes, mentor employees, enforce compliance standards, and foster a culture of accountability and continuous improvement.
Key Responsibilities
- Supervise and support Quality Assurance personnel during 3rd shift operations
- Ensure compliance with FDA regulations, cGMP requirements, company policies, and internal quality standards
- Review and approve quality documentation, including batch records, deviations, non-conformances, and corrective actions
- Partner closely with Manufacturing, Operations, and other cross‑functional teams to resolve quality‑related issues
- Lead investigations related to deviations, non-conformances, and process exceptions
- Monitor production activities to ensure adherence to established procedures and quality requirements
- Drive continuous improvement initiatives focused on quality systems, compliance, efficiency, and employee engagement
- Coach, mentor, and develop team members through performance management, training, and ongoing feedback
- Address employee performance concerns, provide conflict resolution, and ensure compliance with company policies
- Support internal and external audits, inspections, and regulatory activities as needed
- Identify opportunities to strengthen quality systems and improve operational effectiveness
- Ensure SOPs remain current, accurate, and compliant with applicable regulations
Required Qualifications
- 4-5+ years of experience within an
FDA-regulated manufacturing or production environment - Minimum of3 years of Quality Assurance experience
- Experience reviewing and managing:
- SOPs
- Batch records
- Deviations
- Non-conformances
- Quality documentation
- Working knowledge of:
- FDA regulations
- cGMP requirements
- ISO standards
- Lean Manufacturing Principles
- Demonstrated success leading teams in a manufacturing or quality environment
- Experience managing employee performance, accountability, conflict resolution, and policy compliance
- Strong problem‑solving, communication, and organizational skills
Ability to make sound decisions in a dynamic manufacturing environment
Preferred Qualifications
- Experience with in the
dietary supplement, nutraceutical, food, pharmaceutical, or related regulated manufacturing industries - Previous supervisory or people leadership experience
- Experience driving process improvement initiatives and fostering a continuous improvement culture
- Familiarity with CAPA programs, audit support, and quality investigations
Education
- Biology
- Microbiology
- Food Science
- Biotechnology
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