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Audit Supervisor

Job in Columbia, Lexington County, South Carolina, 29228, USA
Listing for: The Ritedose Corporation
Full Time position
Listed on 2026-07-13
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 65000 - 75000 USD Yearly USD 65000.00 75000.00 YEAR
Job Description & How to Apply Below
Location: Columbia

Job Details

Location:

The Ritedose Corporation
- Columbia, SC 29203

Education Level: 4 Year Degree

Salary: $65,000.00 - $75,000.00 / year

Job Category: QA
- Quality Control

Job Description

The Audit Supervisor supports the internal audit program, supplier quality management activities and coordination/execution of customer and regulatory audits. This role is responsible for overseeing day‑to‑day audit activities, ensuring compliance, and guiding audit team members.

Responsibilities
  • Support execution of internal audits according to the Internal Audit Master Plan
  • Monitor and follow up on corrective action implementation related to audit findings
  • Assist in the oversight of the supplier quality management process
  • Conduct supplier audits, including on-site inspections when required
  • Maintain records of audits performed and assist in scheduling repeat audits
  • Support coordination and tracking supplier quality alerts
  • Participate in regulatory and customer audits and assist with audit readiness activities
  • Perform trending of audit findings and report opportunities for improvement to management
  • Maintain current knowledge of applicable regulations and guidance documents
  • Provide guidance and day‑to‑day direction to audit team members
Qualifications
  • Bachelor's degree in Pharmacy, Chemistry, Biology or related field
  • 3-5 years’ experience in the pharmaceutical manufacturing industry with a quality background
  • Working knowledge of cGMP/21

    CFR regulations
  • ASQ Certified Quality Auditor (CQA) or ability to obtain certification within 12 months of hire
  • Experience supporting FDA or regulatory audits
  • Proficient with word processing and database software
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