Complete Genomics is hiring: Reagent Manufacturing Associate in San Jose

This range is provided by Complete Genomics. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $60,000.00 /yr - $80,000.00 /yr Direct message the job poster from Complete Genomics Are you excited to work hands-on with next-generation sequencing technologies that directly impact human health? Do you thrive in a structured, quality-driven manufacturing environment where collaboration, precision, and continuous improvement matter every day? Do you value diversity, open communication, and teamwork as core drivers of success? As a Reagent Manufacturing Associate , you will support the production of high-quality reagents used in Complete Genomics’ next-generation sequencing platforms. This role spans entry-level through early-career professionals, with responsibilities and autonomy aligned to experience, training, and demonstrated performance. WHAT YOU WILL BE DOING Execute reagent manufacturing operations by following established SOPs to ensure accuracy, consistency, throughput, and product quality. Operate and monitor manufacturing equipment including reagent preparation and liquid handling instrumentation, escalating issues or deviations as appropriate. Apply scientific principles in biochemistry, biology, and chemistry to support routine manufacturing activities and resolve common process challenges. Support operational excellence initiatives by participating in standard work, 5S, and continuous improvement efforts within the manufacturing environment. Perform general laboratory operations such as inventory management, supply restocking, and maintenance of clean and organized work areas. Document manufacturing activities accurately using LIMS and other manufacturing systems in compliance with quality and regulatory requirements. Collaborate cross-functionally with manufacturing, formulation, and support teams to meet production goals and key performance indicators (KPIs). Ensure regulatory and safety compliance by adhering to ISO, cGMP, and laboratory safety standards at all times. Maintain an audit-ready work environment through proper documentation, labeling, and adherence to established procedures. WHERE YOU WILL WORK Location: San Jose, CA (On-site) Travel: Minimal; occasional travel may be required for training or internal meetings WHAT YOU WILL BRING US 1 to 3+ years of hands‑on experience in scientific or manufacturing environments within biotechnology, molecular biology, or other regulated laboratory settings. Familiarity with quality and regulatory standards such as ISO and/or cGMP, with the ability to work effectively in compliance-driven environments. Experience operating laboratory or manufacturing equipment including reagent preparation tools and liquid handling systems. Strong documentation and data integrity practices with exceptional attention to detail and accuracy. Experience working within SOP-driven workflows and utilizing manufacturing systems such as LIMS or similar electronic documentation tools. Ability to collaborate effectively across teams including manufacturing, formulation, and operational support functions. Proficiency with standard productivity tools including Microsoft Office applications and general computer systems. ABOUT YOU Detail-oriented and quality-driven , with a strong commitment to accuracy and compliance. Disciplined and reliable , able to consistently follow procedures and meet production expectations. Proactive and adaptable , with a continuous improvement mindset. Collaborative and communicative , valuing teamwork and shared accountability. Motivated to learn and grow , with interest in advancing within manufacturing operations. WHAT YOUR EDUCATION LOOKS LIKE Bachelor’s degree in Chemistry, Biology, or a related scientific field; or an equivalent combination of education and relevant industry experience. Prior exposure to Next Generation Sequencing (NGS) technologies is highly desirable. PHYSICAL REQUIREMENTS & WORK ENVIRONMENT This role requires the ability to perform essential job functions in a manufacturing and laboratory environment. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Ability to stand and move within a manufacturing or laboratory environment for extended periods of time. Ability to lift, carry, push, or pull materials weighing up to 45 pounds, with or without reasonable accommodation. Ability to perform repetitive tasks involving manual dexterity, including handling laboratory tools, reagents, and equipment. Ability to work safely with chemicals, reagents, and laboratory equipment while wearing appropriate personal protective equipment (PPE). Ability to follow safety procedures and work in environments with noise, temperature variation, and controlled cleanroom or laboratory conditions. HOW WE WILL REWARD YOU The base salary range for this position will be $60,000 to $80,000 per year , commensurate with level, experience, and qualifications . This position is eligible for an annual bonus plan as a thank‑you for your hard work and contributions. Additional benefits include: Annual gym membership reimbursement to support your health and wellness Employee discount program We offer eligible employees and their dependents (including domestic partners) a comprehensive and competitive benefits package, with Complete Genomics contributing to the cost, including: Medical, Dental, and Vision Coverage Life and AD&D Insurance Short-Term and Long-Term Disability Insurance Voluntary Life and AD&D Insurance Health Savings Account (HSA) Flexible Spending Accounts (FSA) Domestic Partner Benefits Commuter Program Employee Assistance Program 401(k) Retirement Plan Education Assistance 20 PTO days and 11 paid holidays per year Complete Genomics provides equal employment opportunity without regard to race, color, religion, sex, national origin, sexual orientation, gender identity and/or expression, age, disability, veteran or uniformed service status, or any other characteristic protected by applicable law. Seniority level: Associate. Employment type: Full-time. Job function: Manufacturing, Production, and Quality Assurance. #J-18808-Ljbffr