QA Auditor I — GMP & In-Process Quality Advocate

Aveva Drug Delivery Systems; Fort Lauderdale (FL); Sur place; USD 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

Medical Insurance

Dental Insurance

Vision Insurance

Paid Time Off

401k with employer match

Holidays

Résumé du poste

Aveva Drug Delivery Systems is a pharmaceutical manufacturer focused on innovative drug delivery technologies. The QAIP Auditor I supports Manufacturing, Packaging, R&D, Technical Operations, Engineering and QC to ensure product quality and compliance.

This role conducts on-line batch record reviews, room clearances, and in-process audits to keep the facility audit-ready and compliant with cGMP, SOPs, and quality standards. Strong attention to detail is essential.

Qualifications

• High school diploma or equivalent required; two years of college preferred.
• Two to four years of related experience in pharmaceutical manufacturing or related field.

Responsabilités

• Ensure GMP compliance throughout the facility.
• Approve Shipper labels/roll labels, and clinical labels.
• On-line batch record review and product specifications verification.

Connaissances

QA auditing

cGMP compliance

SOPs

Batch records

Attention to detail

Formation

High School Diploma

Two years of college

Outils

JD Edwards ERP

Description du poste

Aveva Drug Delivery Systems is a pharmaceutical manufacturer focused on innovative drug delivery technologies. The QAIP Auditor I supports Manufacturing, Packaging, R&D, Technical Operations, Engineering and QC to ensure product quality and compliance.

This role conducts on-line batch record reviews, room clearances, and in-process audits to keep the facility audit-ready and compliant with cGMP, SOPs, and quality standards. Strong attention to detail is essential.