SQA Services, Inc.
Quality Auditor - Pharma & EPA Auditor (1-2 Day Audits)
SQA Services, Inc., Jacksonville, Florida, United States, 32290
Quality Auditor - Pharma & EPA Auditor (1-2 Day Audits)
Base pay range: $1,400.00/daily - $1,400.00/daily
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 U.S. 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
Note: 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.
$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.
Get notified about new Quality Auditor jobs in Jacksonville, FL.
#J-18808-Ljbffr
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 U.S. 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
Note: 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.
$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.
Get notified about new Quality Auditor jobs in Jacksonville, FL.
#J-18808-Ljbffr