QA/QC Inspector I: Life Sciences & Medical Devices

Pall Corporation; Timonium (MD); Sur place; USD 33 000 - 39 000; Plein temps

Résumé du poste

Pall Corporation is seeking a QA/QC Inspector I for our on-site operations in Timonium, MD. The role involves verifying and validating products against requirements across all QA processes, with training at the Timonium site and routine overtime.

Shift is Monday–Friday, 6:00 AM–2:30 PM. Responsibilities include ensuring filter media and cartridges meet specs, supporting production inspections, and performing final product inspections prior to shipment.

Qualifications

• High School Diploma or GED required.
• Minimum two (2) years of quality inspection experience in a manufacturing environment operating under ISO 9001 and/or ISO 13485.
• Proficient in Microsoft Office and ERP systems such as SAP or equivalent.

Responsabilités

• Ensure melt‑blown filter media, sub‑assemblies, and finished cartridges meet internal specifications, customer requirements, and applicable regulatory standards.
• Support extrusion, assembly, and finishing operations through timely inspection, testing, and nonconformance management. Protect product integrity by maintaining compliance with the site Quality Management System (ISO / regulated manufacturing environment).
• Perform final inspection of finished products in accordance with approved specifications, inspection procedures, sampling plans, and quality documentation, verify that finished products meet visual, functional, and performance requirements prior to release. Inspect product characteristics related to integrity, sealing, leak prevention, and overall compliance to ensure product is acceptable for shipment to the customer.

Connaissances

Quality inspection

MS Office

SAP / ERP

Formation

High School Diploma or GED

Outils

SAP

ERP systems

Description du poste

Pall Corporation is seeking a QA/QC Inspector I for our on-site operations in Timonium, MD. The role involves verifying and validating products against requirements across all QA processes, with training at the Timonium site and routine overtime.

Shift is Monday–Friday, 6:00 AM–2:30 PM. Responsibilities include ensuring filter media and cartridges meet specs, supporting production inspections, and performing final product inspections prior to shipment.