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Quality Lab Technician - GMP​/QA & Data Analysis

Job in Mountain View, Santa Clara County, California, 94039, USA
Listing for: Canon Medical Diagnostics USA Inc
Full Time position
Listed on 2026-05-26
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager
  • Manufacturing / Production
    QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below

The QA Lab Assistant is located in Mountain View, CA. This is a full-time position with the following benefit options:
Medical, Dental, Vision, FSA, HSA, Life Insurance, 401K with company match, Pet Insurance, etc..

This position will be responsible for in-process/ final product testing and disposition using an MRP system. This role requires tasks to be completed in a timely manner and work assignments to be reprioritized based on the needs of the manufacturing schedule. The preferred candidate will have knowledge of cGLP with an understanding of equipment calibration.

Essential Duties and Responsibilities:
  • Follow detailed procedures and processes.
  • Inspect, test, and release in-process and final product in a timely manner.
  • Approve materials and in-process parts in MRP.
  • Identify non-conforming materials and protocol / procedural errors.
  • Evaluate analytical results and determine conformance to specification.
  • Identify deviations and out of specifications events and document test results, problems and other relevant information.
  • Maintain laboratory equipment to assure accuracy and confidence
Position Requirements (Knowledge, skills and abilities required to perform satisfactorily in the position):
  • Ability to manage tasks from beginning to end within established timeline.
  • Ability to work independently and cohesively in a team environment.
  • Ability to calculate using algebra, statistics, weights / measures and the metric system and apply logic during data analysis.
  • Ability to use Microsoft Office (Outlook, Excel, Word) and Visio.
  • Ability to use micro-centrifuges.
  • Ability to communicate in English (verbal and written).
  • Basic understanding of 21 CFR 820, ISO 13485. (preferred)
  • Knowledge of cGLP/GDP. (preferred)
  • Effective problem-solving and decision‑making skills.
  • Performs additional duties as necessary
Education and Experience:
  • AS /BS Degree (preferred/not required)
  • Prefer working knowledge in quality control environment and 2 years of experience in FDA regulated manufacturing environment
Supervisory Responsibility:

This position has no supervisory responsibilities.

  • Laboratory Environment
  • Exposure to blood‑borne pathogens and hazardous chemicals.
  • Exposure to a cold room (2-8°C) environment for up to 30 minutes continuously at a time
  • Must wear protective equipment such as safety glasses, laboratory coats, gloves, hairnets, face shields and any relevant equipment deemed as necessary.
Physical Demands:
  • Ability to lift up to 30 pounds (totes/containers)
  • Ability to work in a cold room (2-8°C) environment for up to 30 minutes continuously at a time
  • Prolonged viewing of computer screen
  • Frequent use of mouse and keyboard
  • Ability to sit or stand, up to 2 hours continuously at a time and up to 8 hours or more in a day
  • Specific vision abilities include close vision, and the ability to adjust focus
Position type and expected hours of work:

Full time

Travel Demands:

N/A

Other Duties:

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

  • Regularly cleans and maintains a neat and organized work area
  • Participates in continuous improvement activities
  • Participates in the development, implementation and maintenance of Quality Systems and other Quality Assurance activities
  • Coordinates work assignments to meet production timelines
  • Performs customer complaint testing
  • Assists in writing inspection protocols and validations
  • Maintains laboratory inventory and orders supplies, as needed

    Performs basic equipment inspections and troubleshooting
  • Performs initial troubleshooting of issues which arise during routine analysis
  • Perform document changes and revisions.
Affirmative action plan/equal employer opportunity (AAP/EEO) statement:

Canon Medical Diagnostics USA, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, marital status, pregnancy, sex, gender expression or identity, sexual orientation, citizenship, genetics or any other legally protected class. In addition to federal law requirements, Canon Medical Diagnostics USA , Inc.

complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

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