Guardant Health is hiring a
Reagent Manufacturing Associate I

Summary

Join Guardant Health as a Reagent Manufacturing Associate I and contribute to the manufacturing of reagents, assembly of kits, and qualification of assigned reagents following Good Manufacturing Practices.

Requirements

• High School Diploma with 2 years of experience in related field; OR Minimum of Associate degree or equivalent; OR Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field preferred
• Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred
• Previous laboratory work experience preferred
• Previous GMP laboratory work experience preferred
• Ability to proactively communicate consistently, clearly, and honestly
• Strong computing skills
• Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed
• Able to integrate and apply feedback in a professional manner
• Ability to work as part of a team

Responsibilities

• Manufacture reagents, assemble kits, and qualify assigned reagents according to SOP
• Document reagent manufacturing activities following cGMP
• Perform equipment maintenance according to the laboratory’s standard operating procedures
• Maintain sufficient inventory of material, supplies and equipment in the laboratory for performance of duties
• Clean racks and other laboratory supplies
• Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
• Perform clerical work and maintain Reagent Manufacturing and Quality Control documents as necessary
• Assist with managing and ensuring sufficient inventory of reagents in the laboratories of Clinical Operations
• Assist with troubleshooting of manufactured reagents
• Assist in the revision and development of reagent manufacturing SOPs and forms
• Participate in interdepartmental activities with Clinical Operations, Quality Assurance, Quality Control and Supply Chain Management to ensure qualified reagents are available for use at all times
• Assist in the inspection preparation activities as needed
• Perform other duties as assigned
• Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer