Quality Engineer III

2 days ago

Redwood City, CA, United States LanceSoft Inc Full-time $85,000 - $110,000
  • 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/ISO14971.

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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