Production Floor QA Specialist – Hands-On Quality

Automatic Data Processing, Inc.; Los Angeles (CA); Sur place; USD 34 000 - 44 000; Plein temps

Résumé du poste

Puretek is seeking a hands-on Quality Assurance Coordinator to provide QA support across production, compounding, filling, packaging, and material handling. In this role you will perform routine and random QA spot checks, verify SOPs and batch records, monitor contamination risks, and ensure adherence to cGMP and quality standards on the manufacturing floor.

The ideal candidate has a degree in a related science and 5+ years in GMP environments, with strong attention to detail and clear

Qualifications

• Associate's or Bachelor's degree in Chemistry, Biology, Pharmaceutical Science, Food Science, Quality, or a related field preferred.
• 5+ years of experience in Quality Assurance, Quality Control, or manufacturing within a GMP-regulated environment preferred.
• Working knowledge of cGMP and Good Documentation Practices.
• Strong attention to detail and observational skills.
• Ability to identify potential contamination and quality risks.
• Strong written and verbal communication skills.
• Ability to work independently and interact effectively with Production and Quality personnel.
• Comfortable spending a significant portion of the workday on the manufacturing floor.

Responsabilités

• Perform routine and random QA walkthroughs and spot checks in production, compounding, filling, packaging, and warehouse areas.
• Verify compliance with approved SOPs, batch records, work instructions, and cGMP requirements.
• Monitor raw material handling and charging activities to help prevent foreign-material contamination.
• Inspect production areas for potential sources of contamination, including plastic, cardboard, fibers, equipment debris, damaged gaskets, packaging fragments, and other foreign particles.
• Verify proper handling and opening of raw material bags and liners.
• Confirm that tanks, vessels, containers, and exposed products are properly protected from contamination.
• Monitor gowning, hygiene, housekeeping, equipment cleanliness, line clearance, and material status controls.
• Verify completion of required in-process checks and documentation.
• Identify GMP deficiencies and communicate observations immediately to Production and QA management.
• Document QA observations and follow up on corrective actions.
• Support investigations, deviations, CAPAs, and customer complaint investigations.
• Assist with trending recurring GMP and foreign-material observations.
• Escalate significant product-quality or contamination risks to QA management.

Connaissances

QA

GMP

cGMP

Documentation

Inspection

Communication

Formation

Bachelor's degree in Chemistry/Biology/Pharmaceutical Science

Description du poste

Puretek is seeking a hands-on Quality Assurance Coordinator to provide QA support across production, compounding, filling, packaging, and material handling. In this role you will perform routine and random QA spot checks, verify SOPs and batch records, monitor contamination risks, and ensure adherence to cGMP and quality standards on the manufacturing floor.

The ideal candidate has a degree in a related science and 5+ years in GMP environments, with strong attention to detail and clear