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Quality Engineer III​/Sr. Quality Engineer

Job in Redwood City, San Mateo County, California, 94061, USA
Listing for: LanceSoft Inc
Full Time position
Listed on 2026-02-24
Job specializations:
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Quality Engineer III / Sr. Quality Engineer
  • Contract
Company Description

JOHNSON & JOHNSON / CALIBRA

Job Description

Title:

Sr. Quality Engineer for Swing Shift

Supervisor: QA Manager

Location:

Redwood City, CA

Purpose of Position:
Supports production of clinical devices and process development. Maintains compliance to Medical Device Directives (MDD), ISO 13485, and Quality System Regulations for Design Controls. Create protocols and reports for a device manufacturing and testing where needed. Perform specific data analysis and trending as required. Provide technical support to Manufacturing and R&D.

Essential Functions
  • Assists in assuring that Good Manufacturing Practice requirements are met, including Design Control.
  • Performs review of production LHR and signoff as required.
  • Reviews currently manufacturing process documentation and records.
  • Works with Quality and Operations to maintain quality requirements in the support of clinical builds.
  • Develops and implements specific testing for existing and new products including supporting process validations.
  • Provides support to manufacturing inspection process development.
  • Researches and provides guidance to the design team regarding standards and regulations applicable to the development project.
  • Perform other duties in quality assurance as directed.
  • Works in accordance with quality system procedures.

Minimum Education:

BS/BA in an Engineering discipline preferred, equivalent combination of education and work experience acceptable.

Minimum Experience:

5 years of experience in Quality Engineering in the medical device industry.

Licenses, Certifications, and Registrations: ASQ Certified Quality Engineer certification preferred.

Other Essential Knowledge, Skills, and Abilities
  • Must have strong oral and written communication skills.
  • Strong knowledge in the use of manufacturing processes used in the medical device industry.
  • Strong knowledge of statistical data analysis.
  • Working knowledge of FDA QSR, EN/ISO 13485 and EN/ISO
    14971.
Working Environment

Job duties are typically performed in an office environment. Overall duties require the ability to stand or sit for lengthy periods of time in a lab. Required duties include utilizing standard office equipment such as a computer, photocopier, and telephone, and reading and writing.

Travel

Some out of town travel may be required for supplier interactions (anticipated to be 10% of time).

Personal Protective Equipment

Latex/rubber/heat resistant gloves, UV eye protection, safety glasses, goggles, respirators, splash aprons, cleanroom gowning wear (smocks, head covers, beard covers, shoes covers).

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