Biochemical Manufacturing Tech

Requirements

• May require some higher education or specialized training/certification, or equivalent combination of education and experience
• 1+ years of relevant experience in a manufacturing environment preferred
• Additional Details
• This job has a full time weekly schedule. Applications for this job will be accepted until at least June 19, 2026 or until the job is no longer posted.
• Travel Required:
• No
• Shift:
• Day
• Duration:
• No End Date
• Job Function:
• Manufacturing

Benefits

Additional Information

Job Description What's it like to work at Agilent in Manufacturing? Watch the video" 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. Job 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. 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. Duties include: 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

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Company Intel

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