Audit Manager

Posted: Tuesday, 16 September 2025
Valid Thru: Thursday, 16 October 2025
Index Requested on: 09/16/2025 19:35:45
Indexed on: 09/16/2025 19:35:45

Location: Columbia, SC, 29203, US

Industry: Manufacturing - Other
Occupational Category: 11-0000.00 - Management
Type of Employment: FULL_TIME

The Ritedose Corporation is hiring!

Description:

The Audit Manager is responsible for the internal audit program, supplier quality management and coordination/execution of customer and regulatory audits.

Responsibilities:

  • Ensure execution of internal audits according to the Internal Audit Master Plan
  • Track the execution of corrective action implementation of audit findings
  • Provide oversight to supplier quality management process
  • Conduct supplier audits including on-site inspections when required
  • Maintain a history of audits performed and schedule repeat audits as required
  • Coordinate and manage supplier quality alerts
  • Coordinate and participate in regulatory and customer audits
  • Perform trending of audit findings and identify opportunities for improvement
  • Maintain current knowledge of regulations and guidance documents
  • Manage and mentor audit personnel

Qualifications:

  • Four year college degree in Pharmacy, Chemistry, Biology or related field
  • 5-10 years’ experience in the pharmaceutical industry with a quality background
  • Thorough knowledge of cGMP/ 21CFR with related experience in regulatory and compliance
  • ASQ Certified Quality Auditor required
  • Experience with FDA audits
  • Proficient with current word processing and database software
  • Strong interpersonal/group skills with ability to motivate and direct others
  • Strong communication skills, verbal and written

Responsibilities:

Please review the job description.

Educational requirements:

  • high school

Desired Skills:

Qualifications:

  • Four year college degree in Pharmacy, Chemistry, Biology or related field
  • 5-10 years’ experience in the pharmaceutical industry with a quality background
  • Thorough knowledge of cGMP/ 21CFR with related experience in regulatory and compliance
  • ASQ Certified Quality Auditor required
  • Experience with FDA audits
  • Proficient with current word processing and database software
  • Strong interpersonal/group skills with ability to motivate and direct others
  • Strong communication skills, verbal and written

Benefits:

Please see the job description for benefits.

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