In-Process QA Auditor I, Pharma

Aveva Drug Delivery Systems; Florida; On-site; USD 28,000 - 40,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k

Paid time off

Paid holidays

Job summary

Aveva Drug Delivery Systems is seeking a QAIP Auditor I to support Manufacturing, Packaging, R&D, Technical Operations, Engineering and QC by performing room and equipment line clearance, visual inspection of finished products, and on-line batch record review. The role ensures the facility remains audit-ready with daily walkthroughs and rigorous adherence to quality standards.

The position requires at least a high school diploma with 2–4 years related experience in pharma manufacturing or

Qualifications

• Excellent written and verbal communication skills in English.
• Proficiency with Microsoft Office products (Word, Excel, Access, PowerPoint).
• Experience with JD Edwards ERP system is a plus.

Responsibilities

• Ensure GMP compliance throughout the facility.
• Enforce cGMP regulations and Aveva’s SOPs.
• Maintain knowledge of Production Manufacturing and Packaging SOPs.
• Monitor the In-Process product defects Tracking, Trending Assessment.

Skills

Attention to detail

Communication skills

Microsoft Office

English proficiency

Education

High School Diploma or equivalent

Two years of college

Tools

JD Edwards ERP

Job description

Aveva Drug Delivery Systems is seeking a QAIP Auditor I to support Manufacturing, Packaging, R&D, Technical Operations, Engineering and QC by performing room and equipment line clearance, visual inspection of finished products, and on-line batch record review. The role ensures the facility remains audit-ready with daily walkthroughs and rigorous adherence to quality standards.

The position requires at least a high school diploma with 2–4 years related experience in pharma manufacturing or