QA In-Process Auditor

Quality Assurance In-Process (QAIP) Auditor I

3rd Shift | 3-Month Contract | Pay Rate: $25/hour

The QAIP Auditor I is responsible for supporting Manufacturing, Packaging, Quality Control, Engineering, and Technical Operations by performing in-process audits, line clearances, batch record reviews, and product inspections to ensure compliance with GMP and quality standards within a pharmaceutical manufacturing environment.

Key Responsibilities

• Perform room and equipment line clearance activities
• Conduct in-process audits within manufacturing and packaging areas
• Review batch records in real time for accuracy and compliance
• Perform visual inspections of finished products
• Collect stability, retain, and inspection samples from production lines
• Support AQL inspections and documentation activities
• Conduct facility walkthroughs to ensure audit readiness and GMP compliance
• Monitor product defects, trending, and quality concerns
• Assist with investigations and escalation of quality issues
• Collaborate with Production and Quality teams to resolve product quality concerns
• Ensure compliance with SOPs, cGMP regulations, and company quality standards
• Support Annual Product Reviews (APR) and reserve sample coordination

Qualifications

• High School Diploma or equivalent required
• 2–4 years of related experience in a pharmaceutical or regulated manufacturing environment preferred
• Experience working with cGMP procedures
• Strong attention to detail and organizational skills
• Ability to manage multiple priorities in a fast-paced environment
• Good written and verbal communication skills
• Proficient with Microsoft Office programs including Word and Excel
• Experience with ERP systems is a plus
• Ability to work effectively in a team environment

#PRO123

Pay: $25.00 per hour

Benefits:

• Dental insurance
• Health insurance
• Vision insurance

Work Location: In person

Salary : $25