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Biomedical Engineer QC Technician

Confidential Client•Consulting
Entry LevelContractOn-Site$40,567
North Richmond, California
16 Hours Ago

The Quality Control Technician role involves investigating and resolving customer complaints related to blood glucose monitoring products by performing physical, chemical, and functional testing. This entry-level position requires adherence to ISO and FDA quality standards, meticulous documentation, and effective teamwork within a controlled manufacturing environment. The technician supports timely complaint resolution through detailed investigation and use of laboratory troubleshooting equipment.

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Description

About Careertakes

👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Scientific & QA.

Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.


Role Overview

This is an entry-level Quality Control / Biomedical Technician role supporting complaint investigations for blood glucose meters, strips, and sensors. The Confidential Client seeks a detail-oriented technician to unpack and process returned products, run routine physical/functional tests, document results in the complaint handling system, and support timely complaint closures. This is an on-site, contract-to-hire position based in North Richmond, CA.


Key Responsibilities

  • Unpack and safely sort returned products by product line.
  • Investigate returned blood glucose meters, strips, and sensors to determine root cause of customer complaints.
  • Perform routine physical, chemical, and functional testing using lab and troubleshooting equipment.
  • Accurately document all investigation activities and results in the Complaint Handling System.
  • Use instruments such as multimeters, oscilloscopes, test fixtures, and microscopes during investigations.
  • Maintain calibration records, ensure test equipment validity, and perform routine maintenance on quality records.
  • Follow written work instructions and SOPs precisely.
  • Enter test data and investigation results into electronic systems with a high level of accuracy.
  • Support organizational goals for timeliness of complaint investigations and closures.
  • Collaborate with team members to resolve issues and suggest process improvements.
  • Communicate investigation status and findings clearly in writing and verbally.

Minimum Qualifications

  • Associate degree (two-year) in Biomedical Science, related scientific discipline, or equivalent technical training; recent graduates with a bachelor’s degree in Biomedical Engineering or related technical field are encouraged to apply.
  • Comfort using lab and troubleshooting tools (multimeters, oscilloscopes, microscopes, test fixtures).
  • Strong documentation skills and proficiency with electronic data entry systems.
  • Ability to follow detailed written instructions and SOPs.
  • Ability to maintain focus and accuracy during repetitive tasks.
  • Good written and verbal communication skills.
  • Ability to work effectively in a team environment.

Preferred Qualifications

  • Experience in the medical device or biotechnology industry.
  • Familiarity with ISO and FDA Quality System requirements (e.g., complaint handling, GMP/QMS).
  • Prior inspection or lab experience in a regulated environment.

Work Environment & Schedule

  • This position is fully on-site at a controlled manufacturing/sterilization facility in North Richmond, CA.
  • Typically scheduled five days per week; may involve standing for extended periods and lifting boxes or materials up to ~25–40 lbs.
  • Strict adherence to safety and quality protocols is required.

Pay & Benefits

  • Pay range: $27.00 - $33.00 per hour (actual compensation depends on qualifications, experience, and other job-related factors).
  • Contract-to-hire opportunity.
  • Benefits for eligible employees may include medical, dental & vision, 401(k), life insurance options, disability coverage, HSA, transportation benefits, Employee Assistance Program, and paid time off — subject to eligibility and plan terms.

Equal Opportunity & Reasonable Accommodations

Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. Reasonable accommodations are available for applicants with disabilities; please notify us if you require an accommodation during the application or interview process.


Equal Opportunity & Hiring Transparency

Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.

If you have questions about how your data is used, please contact us directly.

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