QA Process Engineer

Hardy Diagnostics

$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering or related discipline
  • Minimum three years of experience in a regulated industry
  • At least two years of quality experience in the same field

Responsibilities

  • Maintain and improve quality systems per FDA and ISO 13485
  • Support quality assurance activities like risk management and audits
  • Investigate quality problems to determine root causes and corrective actions
  • Manage non-conforming products with stakeholders for timely resolution
  • Lead resolution of quality issues related to non-conformance and complaints
  • Oversee the deviation review and approval process
  • Support manufacturing with product and process improvements
  • Serve as a subject matter expert for root cause analysis
  • Provide quality engineering support to production and engineering teams
  • Lead test method validation activities and develop sampling procedures

Benefits

  • Educational and training opportunities
  • Profit-sharing programs
  • Employee Stock Ownership Program (ESOP)
  • Recognition as a 'Fit Friendly' business by the American Heart Association
  • Certification as a 'Green Business' by the County of Santa Barbara
Full Job Description
The QA Process Engineer supports compliance with applicable regulatory requirements by maintaining an effective quality management system and implementing continuous improvements. This position is responsible for activities ranging from product development through commercialization. This is a hands-on role where the QA Process Engineer will apply diversified knowledge of engineering, quality principles and practices for medical devices and laboratory use only products.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may

be assigned.
  • Maintains and improves the quality system in accordance with FDA Quality System Regulation and ISO 13485 requirements
  • Supports quality assurance activities, including, but not limited to: Risk Management, internal and external audits, NCMRs and CAPAs
  • Investigates product quality problems (NCs and deviations) and determine root cause, gather and analyze data, and implement corrective actions to reduce or eliminate cause
  • Manages the Control of Non-conforming Products (CNP) in collaboration with the applicable stakeholders, to ensure timely reporting, analysis, and resolution of non-conforming material
  • Leads/supports the resolution of quality issues related to non-conformance reports, deviations, customer complaints and CAPAs
  • Oversee the deviation process for the review and approval of manufacturing deviations
  • Supports manufacturing team in the maintenance and continuous improvement of product and manufacturing processes
  • Leads and administrates the CNP and CRB meeting
  • Serves as subject matter expert for root cause analysis
  • Provides QE support to production, purchasing and engineering
  • Supports/leads test method validation activities and/or other validation activities as needed
  • Develops and initiates sampling procedures and statistical process control methods
  • Other duties/ activities may be necessary to support departmental or company goal

EDUCATION and/or EXPERIENCE
  • Bachelor's degree (B.S./B.A.) in engineering or related discipline
  • Minimum three (3) years of experience working in a regulated industry
  • Minimum two (2) years of experience in quality in a regulated industry


We also help make our employees better by offering a wide range of educational and training opportunities as well as a full line of benefits, including profit-sharing. Our employees eventually become owners through our Employee Stock Ownership Program (ESOP). The dedication and skill of the people who work here have resulted in remarkable success--Inc. Magazine has recognized us as one of the Fastest Growing Private Companies in America. In addition, we are a "Fit Friendly" business as certified by the American Heart Association and a "Green Business" as certified by the County of Santa Barbara.

Similar Jobs

More Jobs at Hardy Diagnostics

  • QA Process Engineer
    $75K — $95K *
    Santa Maria, CA 93458 (Santa Barbara County)
    Pharmaceuticals & Biotech
    In-Person

More Pharmaceuticals & Biotech Jobs

Find similar QA Process Engineer jobs: