Biochemical Manufacturing Associate

Job DescriptionWhat'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:Peform all duties required to plan and produce bulk reagents while maintaining compliance with internal and external quality standards. Provide direct (approximately 50%) and indirect (approximately 50%) manufacturing support, or as needed, to ensure BCP delivery targets are maintained. Duties include:Batch management within Agilent ERP system (creating, combining, scheduling, opening, closing, combining, disposition etc.)Selecting, allocating, and consuming raw materials to batches per product DHRInventory adjustments within Agilent ERP system levels to accurately reflect physical inventoriesStatus labelling for bulk reagents within BCPReagent filtering, mixing, and transfer between production areasHazardous/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 platforms, conductivity, and UV Vis instrumentsGeneral laboratory cleaning and preventative maintenance in accordance with internal proceduresAdherence to GDP requirements in accordance with internal proceduresAbility to stand or sit for long periods of time, routinely bend and reach, and to lift up to 50lbsRegularly access controlled environments such as walk-in cold rooms (2-8C) and walk-in freezers (-20C). Create / revise controlled documentation and product BOM within Agilent PLM per standard operating procedures. Duties include:Create and approve changes (ECO, LCO, ECR) as needed to improve manufacturing instructions in product DHR or testing procedures, and product BOM Work with R&D and Operations development groups on strategic projects and new product introductions. Duties include:Execute process validation procedures and contribute to report generationRepresent BCP in product development and transfer groupsEnsure NPI requirements for BCP are metCoordinate with cross functional stakeholders to drive strategic projects/initiatives to completionContribute to and lead continuous improvement and digital initiatives within BCP and cross-functionally. Support site CI initiatives by completing regular area checks, participating in project planning and execution, and drive workflow optimization throughout production.Histology Support Tasks: Duties may include but are not limited to -Manufacturing (microtomy, cycle counts, QC testing, etc.)PO management and processingLab maintenance/support (cleaning, PM, etc)QualificationsQualifications Required for the JobEducation: High school diploma. May require some higher education or specialized training/certification, or equivalent combination of education and experience. May require specialized training/certification, or equivalent combination of education and experience.Experience: Prior experience in manufacturing environment required (preferably in cGMP settings).Additional DetailsThis job has a full time weekly schedule. Applications for this job will be accepted until at least May 20, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $34.16 - $53.37/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: Manufacturing