Biochemical Manufacturing Tech

Agilent Technologies•Carpinteria, CA

12d•$22 - $35•Onsite

About The Position

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. This role is within the Biochemical Manufacturing department, supporting the production of reagents for various product lines. The position involves working in a GMP environment and requires adherence to quality standards and procedures.

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 perform 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.
Perform 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).