Reagent Manufacturing Associate

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.

$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.

• 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.

• Location: San Jose, CA (On-site)
• Travel: Minimal; occasional travel may be required for training or internal meetings

• 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.

• 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.

• 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.

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…