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Quality Assurance Auditor – GMP

Actalent, Lancaster, SC, United States


Overview

Description
Note:

This section has been refined to present a clear job-focused summary. The original language is preserved where possible.
Summary of the Position: The Quality Assurance Auditor reports to the Supplier Quality and Compliance Manager. This role is responsible for developing and maintaining a strong Internal Compliance program ensuring compliance to applicable regulations. The QAA is required to perform internal and external audits, prioritize audit schedules and corrective actions to the findings identified.
Responsibilities

Manage audit planning, scheduling, and execute internal and external audits for Nutramax Laboratories to assess compliance to the regulations.
Audit external suppliers (CMO’s) and maintain the vendor qualification program including the Approved Vendor List in Qualityze
Manage external vendor(s) responsible for international audits
Manage the Nutramax supplier corrective action request program (SCAR).
Manage all documents relating to audits, vendors, and suppliers in a QMS (Qualityze)
Determine the level of risk of findings identified and follow up on corrective actions ensuring they address the short-term correction as well as the preventive action of the finding.
Develop and implement a performance tracking system and reporting of departmental compliance.
Prioritize work to ensure that audits and reports are completed in a timely manner. Support implementation of CAPA program where necessary.
Train and assist internal departments to understand and comply with Quality and Compliance expectations.
Assess internal audit process by identifying and prioritizing areas of the business where there is a risk of non-compliance and assist in development and/or execute processes or policies to reduce that risk.
Support training and readiness for regulatory inspections.
Provide support to other Quality Assurance team members.
Report audit metrics to Quality Assurance and department management.
Communicate effectively with all levels of the organization and departments within the organization and function within a team environment.
Understand the roles and responsibilities of the Contract Manufacturing Organizations and provide Quality Assurance support for product development, investigations, and CAPAs as required.
Familiar with QA functions in SAP.
Perform other assigned duties as may be required in meeting Quality Assurance and company objectives.
Qualifications & Skills

GMP
CAPA
FDA
ASQ certified
Quality assurance
Education & Experience

B.A. or B.S. in Science or Technical field required.
Experience Level: Intermediate Level
Job Details

Location: This is a Permanent position based out of Lancaster, SC.
Pay: The pay range for this position is $70,000.00 – $90,000.00/yr.
Workplace: This is a fully onsite position in Lancaster, SC.
Application Deadline: This position is anticipated to close on Apr 29, 2026.
Diversity, Equity & Inclusion

Actalent is an equal opportunity employer. Diversity and inclusion are embedded into our culture through: hiring diverse talent; maintaining an inclusive environment through persistent self-reflection; building a culture of care, engagement, and recognition with clear outcomes; ensuring growth opportunities for our people.

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