QC Specialist I: Lab Testing & Cross-Training

Bio-Rad Laboratories; Hercules (CA); Sur place; USD 42 000 - 60 000; Plein temps

Résumé du poste

Bio-Rad Laboratories in California seeks a Quality Control Associate to perform routine laboratory testing and documentation in support of ISO13485 compliant manufacturing. You will execute core assays (SDS-PAGE, ELISA, HPLC, PCR) and assist with data entry in SAP, coordinating with cross-functional teams to ensure timely product release.

The role requires 0–2 years in a life sciences lab, knowledge of GLP/GMP, and proficiency with Microsoft Office.

Qualifications

• Knowledge of GLP and GMP practices is required.
• Proficiency with Microsoft Office suite.
• Experience with ERP systems, SAP preferred.

Responsabilités

• Perform QC testing on incoming and manufactured materials to support release into inventory.
• Document testing activities and results following good documentation practices to ensure ISO13485 compliance.
• Attend Tier 1 daily meetings to report on safety, quality, delivery and inventory updates.
• Support quality control activities toward special manufacturing reagents and consumables.
• Cross-train across multiple product portfolios and assays in QC environments.

Connaissances

GLP/GMP knowledge

Microsoft Office

Formation

Bachelor's degree in life sciences

Outils

SAP

Description du poste

Bio-Rad Laboratories in California seeks a Quality Control Associate to perform routine laboratory testing and documentation in support of ISO13485 compliant manufacturing. You will execute core assays (SDS-PAGE, ELISA, HPLC, PCR) and assist with data entry in SAP, coordinating with cross-functional teams to ensure timely product release.

The role requires 0–2 years in a life sciences lab, knowledge of GLP/GMP, and proficiency with Microsoft Office.