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Quality Engineer- 6-month Contract

CooperCompanies

West Henrietta, NYOnsitePosted 24 days ago$69,584.00 - $92,779.00 per year
ContractMid LevelQuality (QA / QC)Medical Device
Original posting ↗

Summary

This position uses Quality Engineering principles (i.e. Lean, Six Sigma, Advance Problem Solving, and Root Cause Analysis tools and techniques) to develop and optimize systems and processes so that they are aligned with the overall Company strategy and quality system.

Job description

Job Summary

This position uses Quality Engineering principles (i.e. Lean, Six Sigma, Advance Problem Solving, and Root Cause Analysis tools and techniques) to develop and optimize systems and processes so that they are aligned with the overall Company strategy and quality system.

Responsibilities

  • Utilizes quality engineering and lean tools and techniques to establish sampling plans, develop quality plans, conduct and participate in FMEA activities, support reliability engineering activities, conduct process and systems audits and to assist in specification development.
  • Investigates instances of nonconformance and facilitates the determination of root cause and corrective action/preventive action including the effectiveness of these actions.
  • Analyzes routine and test data for improvement opportunities.
  • Participates in the design experiments (DOE's) for process and product improvement and validation testing.
  • Develops and executes validation plans.
  • Supports, consults, trains and leads quality improvement projects.
  • Provides statistical support for sampling plan and analysis, DOEs, Pareto, ANOVA, and SPC applications.
  • Gathers and evaluates distribution center and packaging performance capability and develops criteria to monitor and improve existing processes, as measured by appropriate quality KPIs.
  • Develop personal and departmental performance objectives based upon the facility quality objectives, reporting monthly on progress made against those goals.
  • Support internal and external audits as needed.
  • Oversees and participates in process and product validations to ensure all processes comply with company specifications to include internal quality systems and ISO requirements as well as applicable laws and regulations.
  • Reviews, develops and maintains all associated documentation including risk management files and quality records.
  • Partners with Quality Assurance team to provide oversight regarding Quality Systems and processes.
  • Partners with Quality Assurance team to deliver workshops and training as required.
  • Provides process mapping and modeling, and provides guidance/options.

Qualifications

  • Demonstrated project management and problem-solving skills.
  • Demonstrated communication, facilitation and leadership skills, with the ability to work cross-functionally in a team environment.
  • Applied technical knowledge of Qualitative and Quantitative data analysis, and statistical tools including DOEs.
  • Six Sigma GB/BB or CQE preferred.
  • Must possess the ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or government regulations.
  • Able to write reports, business correspondence, and procedure manuals.
  • Possess the ability to effectively present information and respond to questions from groups of senior managers.
  • Has a working knowledge of Quality System Regulation (21 CFR PART 820, including 21CFR806) and ISO 13485 requirements.
  • Microsoft Windows, Microsoft Excel, Minitab.
  • BAAN, Agile, JDA familiarity a plus.

Experience

Minimum of 3 plus years applicable experience and/or training or equivalent combination of education and experience with medical device distribution and packaging operations.

Education

Bachelor’s degree (B.S.) from four –year college or university in engineering or related discipline; equivalent combination of education and experience may be considered. Certified Quality Engineer, Green Belt or Lean certified preferred.

Requirements

  • Bachelor’s degree (B.S.) in engineering or related discipline
  • Minimum of 3 plus years applicable experience in medical device distribution and packaging operations
  • Demonstrated project management and problem-solving skills
  • Demonstrated communication, facilitation and leadership skills
  • Applied technical knowledge of Qualitative and Quantitative data analysis and statistical tools including DOEs
  • Working knowledge of Quality System Regulation (21 CFR PART 820, including 21CFR806) and ISO 13485 requirements
  • Microsoft Windows, Microsoft Excel, Minitab
  • Six Sigma GB/BB or CQE preferred
  • Certified Quality Engineer, Green Belt or Lean certified preferred
  • BAAN, Agile, JDA familiarity a plus

Company overview

CooperCompanies (Nasdaq: COO) is a leading global medical device company headquartered in San Ramon, California, with a workforce of over 15,000 employees. The company operates through two primary business units: CooperVision and CooperSurgical. CooperVision is a trusted leader in the contact lens industry, focusing on vision correction and improving daily visual experiences for millions worldwide. CooperSurgical specializes in fertility and women's healthcare, providing innovative medical devices and solutions that support reproductive health and family planning. With products sold in over 130 countries, CooperCompanies positively impacts more than fifty million lives annually. The company generates approximately $4.1 billion in annual revenue and maintains a strong global presence, leveraging its expertise in medical device manufacturing to address critical healthcare needs in both vision care and women's health sectors. CooperCompanies is publicly traded and continues to expand its market leadership through strategic acquisitions, product innovation, and operational excellence.

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