Quality Control Technician (Temp)

About Truvian

Want to join a fast-paced, innovative company that is transforming the future of blood testing? Truvian is a healthcare technology company operating at the intersection of diagnostics and consumer technology. We have developed an automated benchtop diagnostic platform that delivers laboratory-quality results in minutes across a broad range of health tests.

Our proprietary, FDA-cleared technology is designed to make blood testing more accessible, convenient, and affordable by providing comprehensive results from a single small blood sample in minutes throughout a broad range of locations. We are continuing to advance our technology’s capabilities to further redefine point-of-care testing and bring high-quality healthcare closer to where patients need it most.

To us, 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 put 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. Come join us as we realize our vision to make routine health testing convenient, affordable, and actionable for today’s connected consumers!

Job Summary

Truvian is seeking a driven Quality Control Technician to support our Quality Control team for approximately 3–6 months. This is a temporary position. This is a hands-on, bench-based position responsible for supporting in-process testing of bulk materials, reagents, consumable kits, and finished products.

The Quality Control Technician will perform testing on Truvian’s automated blood-testing platform by following established standard operating procedures. Responsibilities will include routine operation and maintenance of laboratory equipment, assembly of test components, evaluation of test results, and accurate documentation of observations and results. 

This individual will work closely with Quality Control team members, scientists, engineers, Manufacturing, and other cross-functional partners to support testing, product release, troubleshooting, and laboratory operations. The successful candidate will bring strong attention to detail, sound documentation practices, flexibility, and a team-oriented approach.   This position will report to the Manager, Quality Control. 

Location and Work Arrangements
Location: San Diego, CA (Onsite)
This role requires regular onsite work. We welcome applications from qualified candidates; however, relocation assistance is not provided for this position. Candidates should be located within commuting distance of the office.

Visa Sponsorship
Candidates must be authorized to work in the United States on a full-time basis. Truvian does not currently provide visa sponsorship or support employment-based immigration petitions for this role.  

Work Schedule
This position offers multiple shift and schedule opportunities. Available shifts may include First Shift and Swing Shift, with workweek schedules of Monday–Friday, Tuesday–Saturday, or Wednesday–Sunday or an alternative workweek schedule of four 10-hour days, Sunday through Wednesday.  Final shift and schedule assignments will be based on position availability and business needs.

Here’s Why You Will Love this Job:

• You will have a hands-on, participant-facing role supporting clinical studies at Truvian to generate data that substantiate the performance of Truvian's breakthrough blood testing technology.
• You'll work with a rock-star team of people who are passionate about the work they do and our ability to disrupt healthcare with our innovative products.
• You’ll be part of a team responsible for the company’s growth and product launch.
• You’ll thrive in a fast-paced, dynamic environment where you can implement fresh ideas and new processes and make things happen quickly without a bunch of red tape.
• You’ll have great perks such as generous benefits (Medical/Dental/Vision/EAP/Paid Life Insurance/LTD/401K), accrued vacation, and on-site wellness perks.

What You Will Do

• Perform routine Quality Control testing of bulk materials, reagents, consumable kits, and finished products.
• Operate the Truvian automated blood-testing platform according to approved procedures and training.
• Follow established test methods, standard operating procedures, specifications, and acceptance criteria.
• Evaluate test results and promptly escalate unusual results, discrepancies, or potential quality issues.
• Accurately document observations, activities, and test results in accordance with Good Documentation Practices.
• Support the timely completion, review, and transmission of Quality Control test data.
• Assist with investigations by gathering information, documenting findings, and preparing investigation summaries.
• Perform routine operation, cleaning, and maintenance of laboratory equipment.
• Verify equipment readiness and calibration status before use.
• Assemble test parts, consumables, or other components as required.
• Support troubleshooting activities, assay validation, and other special laboratory projects as assigned.
• Collaborate cross-functionally to support product release and resolve testing or documentation issues.
• Follow current Good Manufacturing Practices and Truvian’s Quality Management System, policies, procedures, and training requirements.
• Help maintain a clean, organized, and safe laboratory environment.
• Assist with restocking laboratory supplies and maintaining inventory.
• Participate in process and operational improvement activities.
• Manage multiple responsibilities and adapt to changing priorities.
• Perform other duties as assigned.

What You Will Bring

Required Qualifications

• Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related scientific discipline, or an equivalent combination of education and relevant experience.
• Minimum of 3 years of Quality Control, laboratory testing, manufacturing testing, or other directly related experience.
• Familiarity with laboratory or quality testing methods.
• Experience following standard operating procedures, test methods, work instructions, or established laboratory protocols.
• Experience documenting laboratory observations and test results accurately and completely.
• Strong organizational and prioritization skills.
• Strong attention to detail and the ability to carefully follow written instructions.
• Ability to recognize defects, discrepancies, and unusual test results.
• Strong verbal and written communication skills.
• Ability to work independently while contributing effectively within a team.
• Ability to manage multiple assignments and complete tasks by established deadlines.
• Flexibility to respond to changing operational demands and priorities.
• Ability to identify and distinguish between colors.

Preferred Qualifications

• Experience in a medical device, diagnostics, biotechnology, pharmaceutical, or other regulated environment.
• Experience working under current Good Manufacturing Practices.
• Familiarity with Quality Management Systems and Good Documentation Practices.
• Experience operating automated laboratory instruments or diagnostic platforms.
• Experience with reagent, consumable, in-process, or finished-product testing.
• Exposure to nonconformance investigations, troubleshooting, product release, or assay validation.

The benchmark requires a scientific degree with a minimum of 3 years of experience, while also allowing equivalent experience. It emphasizes quality testing methods, Quality Management System knowledge, organization, communication, attention to detail, independence, deadline management, and defect recognition.

Supervisory Role
  No

Compensation
$22.00 to $26.00 per hour
The hourly range for this position represents the anticipated range for qualified candidates. Compensation decisions are based on a variety of factors, including relevant experience, skills, education, training, certifications, internal equity, market data, and business needs. The final compensation offered to a successful candidate will be determined based on these factors and the requirements of the role.

Physical Demands and Abilities

• Regularly use hands to handle laboratory materials, equipment, components, and testing supplies.
• Frequently stand, walk, stoop, kneel, crouch, or move within the laboratory.
• Occasionally sit, climb, or balance.
• Lift and move up to 5 pounds repeatedly and safely.
• Possess the close, distance, color, peripheral, and depth vision necessary to perform detailed laboratory work.
• Maintain the ability to adjust focus when inspecting materials, components, and test results.

Interested candidates are encouraged to submit a cover letter along with their resume. The cover letter is an opportunity to highlight how your experience in assay and/or panel architecture aligns with our mission, your approach to technical leadership and cross-functional collaboration, and how your expertise has driven innovation in diagnostic product development and complex assay systems.

Truvian is an Equal Opportunity Employer and is committed to fostering a diverse, inclusive, and respectful workplace. Employment decisions are made based on qualifications, merit, and business needs. Truvian prohibits discrimination, harassment, and retaliation and does not discriminate on the basis of any characteristic protected by applicable federal, state, or local law, including race, color, religion, creed, sex, pregnancy (including childbirth, breastfeeding, and related medical conditions), gender, gender identity, gender expression, sexual orientation, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, marital status, military or veteran status, reproductive health decision-making, or any other legally protected status. 

This policy applies to all aspects of employment, including recruitment, hiring, placement, promotion, compensation, benefits, training, transfers, leaves of absence, disciplinary actions, termination, and all other terms and conditions of employment. Truvian is also committed to providing reasonable accommodations to qualified individuals with disabilities and to applicants and employees with sincerely held religious beliefs, practices, or observances, in accordance with applicable law.