QA In-Process Auditor I - Quality & Compliance

Aveva Drug Delivery Systems Inc; Florida; On-site; USD 52,000 - 68,000; Full time

Job summary

Aveva Drug Delivery Systems Inc seeks an QAIP Auditor I to support Manufacturing, Packaging, R&D, Technical Operations, Engineering, and QC. Responsibilities include room clearance, on-line batch record review, and sampling for stability and retain materials to ensure GMP compliance.

Requirements include high school diploma or equivalent with further college work, strong English communication, and familiarity with MS Office; JD Edwards ERP is a plus.

Qualifications

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

Responsibilities

• Perform room and equipment line clearance and in-process audits.
• Review batch documentation online for compliance and product specs.
• Collect stability and retain samples from production lines.
• Conduct on-line batch record reviews and QA envelope documentation.

Skills

English communication

Attention to detail

Team collaboration

Education

High School Diploma or equivalent, with 2 years college

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Access

JD Edwards ERP

Job description

Aveva Drug Delivery Systems Inc seeks an QAIP Auditor I to support Manufacturing, Packaging, R&D, Technical Operations, Engineering, and QC. Responsibilities include room clearance, on-line batch record review, and sampling for stability and retain materials to ensure GMP compliance.

Requirements include high school diploma or equivalent with further college work, strong English communication, and familiarity with MS Office; JD Edwards ERP is a plus.