Technician Jobs

About The Position

Requirements

• 1+ years of relevant experience in a manufacturing environment preferred
• May require some higher education or specialized training/certification, or equivalent combination of education and experience

Responsibilities

• Formulate bulk reagents and preform in-process QC testing within GMP environment.
• Support production of reagents for Pathology, Artisan, CDx, and other product lines owned by the Carpinteria site within Global Operations – Manufacturing
• Work cross-functionally within Global Operations – Manufacturing to maintain accurate inventory of all raw, WIP, approved materials.
• Assist with production scheduling for BCP department and in collaboration with IC, IP, QC, and FP.
• Preform all duties required to produce bulk reagents while maintaining compliance with internal quality standards.
• Batch management within Agilent ERP system (opening, closing, combining, disposition etc.)
• Selecting, allocating, and consuming raw materials to batches per product DHR
• Inventory adjustments within Agilent ERP system levels to accurately reflect physical inventories
• Status labelling for bulk reagents within BCP
• Reagent filtering, mixing, and transfer between production areas
• Hazardous/toxic material handling and waste disposal in compliance with internal procedures, including use of powder hoods, fume hoods, and personal respirator
• Operation of equipment required for in-process quality control, including pH meters, automated staining platforms, conductivity, and UV Vis instruments
• General laboratory cleaning and preventative maintenance in accordance with internal procedures
• Adherence to GDP requirements in accordance with internal procedures
• Regularly access controlled environments such as walk-in cold rooms (2-8C) and walk-in freezers (-20C)
• Contribute to continuous improvement initiatives within BCP and cross-functionally

Benefits

• Eligibility for bonus
• Stock eligibility
• Benefits