QA Auditor II

Join our team as a Quality Assurance Auditor II and elevate our clinical auditing processes by ensuring regulatory compliance and quality standards. As a QA Auditor II, you will serve as a knowledgeable resource on audit or quality assurance subject matter, auditing various processes such as database audits, clinical study report audits, and more.

Join our team as a Quality Assurance Auditor II and elevate our clinical auditing processes by ensuring regulatory compliance and quality standards. As a QA Auditor II, you will serve as a knowledgeable resource on audit or quality assurance subject matter, auditing various processes such as database audits, clinical study report audits, and more.

• Conduct and/or lead a variety of client, internal, or GxP audits and regulatory inspections as requested by senior management.
• Perform directed site audits, facility, vendor, and/or sub-contractor audits.
• Provide GxP consultation and support to project teams and external clients.
• Lead process audits and may participate as a co-auditor in more complex system audits.
• Perform other types of QA audits or activities, including database audits, clinical study report audits, and sample results tables.
• Serve as a knowledgeable resource to operational departments on audit or quality assurance subject matter.
• Prepare and present audit findings and/or other related information at departmental, internal operations, or client meetings.

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
• Previous QA experience that provides the knowledge, skills, and abilities to perform the job, comparable to 2+ years.
• Thorough knowledge of GxP and appropriate regional research regulations and guidelines.
• Demonstrated proficiency in leading a range of project-based or internal GxP audits and vendor audits to high standards.

• Excellent oral and written communication skills.
• Strong problem-solving, risk assessment, and impact analysis abilities.
• Solid experience in root cause analysis.
• Above average negotiation and conflict management skills.

Work is performed in an office, laboratory, and/or a clinical environment. Exposure to biological fluids with potential exposure to infectious organisms is possible. Exposure to electrical office equipment is common. Personal protective equipment such as protective eyewear and garments is required.

This is a Contract position based out of Richmond, VA.

The pay range for this position is $38.06 - $43.97/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Richmond, VA.

This position is anticipated to close on Sep 26, 2026.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccom for other accommodation options.

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