Quality Auditor - Animal Health & GLP Auditor (1-2 Day Audits)

For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across all industries. We deliver these services by deploying a network of highly skilled associates based throughout the United States and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our competitors.

We’re hiring a pharmaceutical /EPA Auditor. This is a contract opportunity in which you will perform

1-2 day audits

at various suppliers in the US. You are given the flexibility to accept or reject these assignments according to your own availability.

The ideal candidate will have a solid foundation in

21 CFR 210/211 ,

ISO 9001 , and

EPA environmental compliance , and be capable of serving as a

Lead Auditor

on client programs within the U.S.

Key Responsibilities

Conduct

on-site audits

within the

pharmaceutical

industries, with specific attention to

EPA ,

GMP (21 CFR 210/211) , and

ISO 9001

requirements.

Evaluate manufacturing sites for compliance with

environmental regulations

and

Good Manufacturing Practices (GMP) .

Develop audit plans, conduct opening and closing meetings, and deliver detailed audit reports per

SQA and client specifications .

Assess supplier compliance to both

quality

and

environmental

standards.

Collaborate with the

SQA Content Team

to finalize reports and address client questions.

Represent

SQA Services

professionally in all supplier and client interactions.

Required Qualifications

Minimum

5 years of experience

in quality auditing within the

Pharmaceutical

or

related regulated industries .

Must have conducted at least

5 audits as a Lead Auditor .

Proven experience auditing against

21 CFR 210/211 ,

ISO 9001 , and

EPA

standards.

Knowledge of

environmental compliance ,

waste handling , and

HSE (Health, Safety & Environmental)

principles.

Strong written and verbal communication skills.

Availability for

at least two audits per month

(additional REQs may be opened for higher capacity).

Willingness to travel for audits across the

Southeast U.S.

(Florida, Georgia, Alabama, the Carolinas) and occasionally to other U.S. regions.

Preferred Qualifications

Experience auditing

pharmaceutical

manufacturing facilities.

Background in

EPA environmental site compliance ,

ISO 14001 , or

HSE auditing .

Lead Auditor certifications in

ISO 9001 ,

ISO 14001 , or

GMP .

Familiarity with

environmental permitting, waste stream control, or contamination prevention .

$1,400 - $1,400 a day

$1,400 USD per 1-day

audit

(inclusive of preparation, travel, audit execution, reporting, and follow-up).

Travel expenses reimbursed

at cost with receipts per SQA travel policy.

Flexible, project-based opportunity — you may accept or decline audit assignments based on your schedule.

SQA is an Equal Opportunity Employer. Employment is based on merit and qualifications, and is not influenced by race, color, religion, gender, national origin, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.

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