Quality Assurance Auditor - GMP

The Quality Assurance Auditor develops and maintains a robust internal compliance program that ensures adherence to applicable regulations in an FDA-regulated, cGMP manufacturing environment. This role plans and conducts internal and external audits, oversees supplier and vendor qualification programs, manages corrective actions, and supports regulatory inspection readiness. The position works closely with internal departments and external partners to drive continuous improvement in quality and compliance while contributing to a strong, values-driven company culture.

Responsibilities

• Plan, schedule, and execute internal and external audits to assess compliance with applicable regulations and company quality standards.
• Audit external suppliers, including contract manufacturing organizations (CMOs), and maintain the vendor qualification program, including the Approved Vendor List within Qualityze.
• Manage external vendors responsible for conducting international audits and ensure their activities align with company quality and compliance expectations.
• Oversee the supplier corrective action request (SCAR) program and ensure timely and effective resolution of supplier-related quality issues.
• Manage and maintain all documents related to audits, vendors, and suppliers within the Quality Management System (QMS), including Qualityze.
• Assess audit findings, determine the level of risk, and follow up on corrective and preventive actions to ensure both short-term corrections and long-term preventive measures are implemented.
• Develop and implement performance tracking systems and reporting tools to monitor departmental compliance and audit performance.
• Prioritize workload to ensure that audits, reports, and follow-up activities are completed accurately and on time.
• Support the implementation of the Corrective and Preventive Action (CAPA) program where necessary, including investigations and follow-up activities.
• Train and assist internal departments to understand and comply with quality and compliance expectations, policies, and procedures.
• Assess the internal audit process by identifying and prioritizing areas of risk for non-compliance and assist in developing or executing processes and policies to reduce that risk.
• Support training and readiness activities for regulatory inspections, including preparation of documentation and coordination with relevant departments.
• Provide ongoing support to other Quality Assurance team members to meet departmental and company quality objectives.
• Report audit metrics and trends to Quality Assurance and departmental leadership to support data-driven decision-making.
• Communicate effectively with all levels of the organization and across departments, fostering collaboration and a strong team environment.
• Understand the roles and responsibilities of contract manufacturing organizations and provide Quality Assurance support for product development, investigations, and CAPAs as required.
• Utilize and remain familiar with Quality Assurance functions in SAP to support quality and compliance activities.
• Perform other duties as assigned to support Quality Assurance and overall company objectives.

• Minimum of 5 years of Quality Assurance auditing experience in a cGMP environment.
• Minimum of 5 years of external vendor and supplier compliance auditing experience within an FDA-regulated industry.
• Proven experience conducting both internal and external audits.
• Experience working in manufacturing environments, including exposure to clean rooms.
• Strong understanding of cGMP principles and FDA-regulated industry practices.
• Proficiency with computer software applications, including the Microsoft Office Suite.
• Ability to stand, walk, push, and pull in a variety of environments, including manufacturing areas and clean rooms.
• Ability to wear all required Personal Protective Equipment (PPE) appropriate to the auditing environment.
• Ability to travel approximately 20–30% for domestic audits, sometimes with limited notice, and flexibility for potential international travel as needed.
• Strong adaptability and flexibility in a dynamic quality and compliance environment.
• Demonstrated initiative and a proactive approach to identifying and resolving quality and compliance issues.
• Excellent interpersonal skills with the ability to build and maintain strong relationships with operations teams and suppliers.
• B.A. or B.S. degree in a science or technical field.

• Knowledge of FDA regulations 21 CFR Parts 210, 211, and 507, as well as Dietary Supplement Regulations 21 CFR 111, is preferred.
• ASQ Certified Quality Auditor (CQA) certification is preferred.
• Experience managing supplier corrective action request (SCAR) programs.
• Experience supporting and implementing CAPA programs, including investigations and preventive actions.
• Familiarity with Quality Management Systems, particularly Qualityze, for managing audits, vendors, and supplier documentation.
• Experience with QA-related functions and processes in SAP.
• Strong communication skills, both written and verbal, with the ability to present audit findings and metrics clearly to leadership.
• Ability to develop and implement performance tracking systems and compliance reporting.
• Commitment to values such as honesty, integrity, commitment, and responsibility.

This is a full-time, first-shift position with typical hours of Monday through Friday, 8:30 a.m. to 5:00 p.m. The role operates in a mixed office and manufacturing environment, including time spent in clean rooms and on the production floor, where wearing appropriate Personal Protective Equipment (PPE) is required. Travel of approximately 20–30% is expected for domestic audits, with occasional short notice and potential international travel as needed. The company fosters a strong, values-driven culture that emphasizes honesty, integrity, commitment, and responsibility, and offers opportunities to work cross-functionally and "wear many hats" within the Quality Assurance function. The work environment supports collaboration with operations, suppliers, contract laboratories, and contract manufacturing organizations, and provides a supportive culture with discretionary bonus potential and relocation assistance.

Job Type & Location

This is a Permanent position based out of Lancaster, SC.

The pay range for this position is $70000.00 - $90000.00/yr.

Featured benefits:Medical insuranceVision insuranceDental insurance401(k)Disability insuranceTuition assistanceChild care support

This is a fully onsite position in Lancaster,SC.

This position is anticipated to close on May 11, 2026.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is 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

Actalent is an equal opportunity employer.

About Actalent

Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.