GH
Reagent Manufacturing Associate
Redwood City, CA
Sponsorship not specified$30k-$41kDetected 4 days ago
Supply ChainPatient CareClinical Laboratory TechniquesGMPCommunicationCollaboration
About the role
- The Reagent Manufacturing Associate (RMA) I is responsible for manufacturing reagents, assembling kits, and qualification of assigned reagents following Good Manufacturing Practices and documenting events following current Good Documentation Practices.
- Manufacture reagents, assemble kits, and qualify assigned reagents according to SOP;
- Clean racks and other laboratory supplies;
Responsibilities
- 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;
- 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;
- Perform other duties as assigned; and
- If you need support, please reach out to Peopleteam@guardanthealth.com
- We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires.
Requirements
- Ability to proactively communicate consistently, clearly, and honestly.
- Employee may be required to lift routine office supplies and use office equipment.
- Ability to sit for extended periods of time.
- A background screening including criminal history is required for this role.
- Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred.
- 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.
- AI & Digital Fluency
- Demonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the efficiency, effectiveness, and quality of work.
- Hybrid Work Model: This section is applicable to onsite employees who are eligible for hybrid work location as specified by management and related policies. Guardant has defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. All U.S. employees who live within 50 miles of a Guardant facility will be required to be onsite on Mondays, Tuesdays, and Thursdays. We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires. At Guardant, our work model has created flexibility for better work-life balance while keeping teams connected to advance our science for our patients.
Nice to have
- High School Diploma with 4 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.
- Previous laboratory work experience preferred.
- Previous GMP laboratory work experience preferred.
Compensation
- $25 - $35If the role is performed in Colorado, the pay range for this job is: $27 - $37
Benefits
- Guardant Health is a leading precision oncology company focused on guarding wellness and giving every person more time free from cancer.
- This range does not include benefits or, if applicable, bonus, commission, or equity.
Equal opportunity
- All your information will be kept confidential according to EEO guidelines.
This listing is sourced directly from GH's careers page and normalized into a canonical job model.