QA In-Process Auditor I: GMP Compliance

Aveva Drug Delivery Systems; Town of Florida (NY); On-site; USD 29,000 - 40,000; Full time

Job summary

Aveva Drug Delivery Systems in Miramar, FL is seeking a Quality Assurance In-Process (QAIP) Auditor I to support Manufacturing, Packaging, R&D, Technical Operations, Engineering and QC. The role involves room and equipment line clearance, visual inspection, sampling, and real-time batch record reviews to ensure conformance to quality standards.

The candidate will perform on-line audits, engage in AQL planning, and help maintain audit readiness.

Qualifications

• Education: High School Diploma or equivalent, with 2 years of college.
• 2-4 years related experience or training.
• Experience with cGMP in pharmaceutical/manufacturing environments preferred.
• Proficient in English communication (written and oral).

Responsibilities

• Ensure GMP compliance throughout the facility.
• Enforce cGMP regulations and SOPs.
• Maintain knowledge of production and packaging SOPs.
• Approve labels and packaging documentation.
• Perform room and equipment line clearance for packaging.
• Conduct on-line batch record reviews for compliance.

Skills

English communication

MS Office

Attention to detail

Teamwork

Education

High School Diploma or equivalent

2 years college

2-4 years related experience

Tools

JD Edwards ERP

Job description

Aveva Drug Delivery Systems in Miramar, FL is seeking a Quality Assurance In-Process (QAIP) Auditor I to support Manufacturing, Packaging, R&D, Technical Operations, Engineering and QC. The role involves room and equipment line clearance, visual inspection, sampling, and real-time batch record reviews to ensure conformance to quality standards.

The candidate will perform on-line audits, engage in AQL planning, and help maintain audit readiness.