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QC Lab Technician (temp)
Truvian SciencesSan Diego, United Statesfull_timeVerifiedPosted 2 Oct 2024
💰 $38,000/yr
About the role
ABOUT
Want to work for a fast-paced and disruptive company that is working to revolutionize blood testing? Truvian is a healthcare company at the intersection of diagnostics and consumer tech. We are developing an automated benchtop diagnostic system to provide lab-accurate results in 30 minutes for a comprehensive suite of health tests. Our proprietary approach, for which we are seeking FDA clearance, is intended to fulfill the promise of delivering accessible and affordable blood testing from one small blood sample in minutes in a retail setting or private clinic.
Our work at Truvian is more than a job—it’s a mission. We are a culture dedicated to discovery and empowerment. We are trailblazers on the path to putting health information where it belongs—in the hands of the individual. We are partners in the belief that talented people working as a team can make every day an adventure. Join us as we realize our vision to make routine health testing convenient, affordable, and actionable for today’s connected consumers!
JOB SUMMARY
Truvian seeks a driven (temp) QC Lab Technician to join our Quality Control team. As a QC Lab Technician, you'll perform various laboratory tasks within a team environment, specifically running reagents and consumable kits on Truvian’s automated blood testing platform. This is a hands-on bench position with primary responsibilities including, but not limited to, testing on the Truvian instrument following specific standard operating procedures, routine operation and maintenance of laboratory equipment, assembly of test parts as required, and documentation of observations and test results. This individual will collaborate with scientists and engineers to execute experiments by operating the Truvian Platform. The successful candidate will possess strong attention to detail skills and a team player mentality. This is an exciting opportunity to be part of a dynamic team and contribute to advancing healthcare technology, making a real difference in the lives of many.
The successful candidate must complete training to ensure compliance with current Good Manufacturing Practices and other regulatory requirements. In addition, this individual will adhere to all requirements of established quality systems.
This is a temporary, entry-level position that requires one to be onsite. The required hours of availability are a 6 a.m. start time and availability until 9 a.m. at the earliest. The position is for a three-month term, with the possibility of an extension based on performance and company needs.
Join our exciting team focused on making routine health testing convenient, affordable, and actionable for today’s connected consumers. Submit your resume and a cover letter to be considered.
WHAT YOU WILL DO:
Want to work for a fast-paced and disruptive company that is working to revolutionize blood testing? Truvian is a healthcare company at the intersection of diagnostics and consumer tech. We are developing an automated benchtop diagnostic system to provide lab-accurate results in 30 minutes for a comprehensive suite of health tests. Our proprietary approach, for which we are seeking FDA clearance, is intended to fulfill the promise of delivering accessible and affordable blood testing from one small blood sample in minutes in a retail setting or private clinic.
Our work at Truvian is more than a job—it’s a mission. We are a culture dedicated to discovery and empowerment. We are trailblazers on the path to putting health information where it belongs—in the hands of the individual. We are partners in the belief that talented people working as a team can make every day an adventure. Join us as we realize our vision to make routine health testing convenient, affordable, and actionable for today’s connected consumers!
JOB SUMMARY
Truvian seeks a driven (temp) QC Lab Technician to join our Quality Control team. As a QC Lab Technician, you'll perform various laboratory tasks within a team environment, specifically running reagents and consumable kits on Truvian’s automated blood testing platform. This is a hands-on bench position with primary responsibilities including, but not limited to, testing on the Truvian instrument following specific standard operating procedures, routine operation and maintenance of laboratory equipment, assembly of test parts as required, and documentation of observations and test results. This individual will collaborate with scientists and engineers to execute experiments by operating the Truvian Platform. The successful candidate will possess strong attention to detail skills and a team player mentality. This is an exciting opportunity to be part of a dynamic team and contribute to advancing healthcare technology, making a real difference in the lives of many.
The successful candidate must complete training to ensure compliance with current Good Manufacturing Practices and other regulatory requirements. In addition, this individual will adhere to all requirements of established quality systems.
This is a temporary, entry-level position that requires one to be onsite. The required hours of availability are a 6 a.m. start time and availability until 9 a.m. at the earliest. The position is for a three-month term, with the possibility of an extension based on performance and company needs.
Join our exciting team focused on making routine health testing convenient, affordable, and actionable for today’s connected consumers. Submit your resume and a cover letter to be considered.
WHAT YOU WILL DO:
- Perform in-process and final product testing following Standard Operating Procedures
- Ensure products are tested to meet the highest quality standards as determined by performance specifications
- Effectively implement and maintain Truvian’s company standard operating procedures for Quality Control
- Understands test results and pursues clarification of unusual results. Develops and uses the system to anticipate and recognize errors. Resolves discrepancies and reports results
- Prepares investigation summaries and reports
- Creates, revises, and updates standard operating procedures as needed
- May contribute to special troubleshooting projects and assay validations
- Works cross-functionally to rele
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