CooperVision
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Quality Engineer
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CooperVision Direct message the job poster from CooperVision Job Description CooperVision, a division of CooperCompanies (NASDAQ:COO), is one of the world’s leading manufacturers of soft contact lenses. The Company produces a full array of daily disposable, two-week and monthly contact lenses, all featuring advanced materials and optics. CooperVision has a strong heritage of solving the toughest vision challenges such as astigmatism, presbyopia and childhood myopia; and offers the most complete collection of spherical, toric and multifocal products available. Through a combination of innovative products and focused practitioner support, the company brings a refreshing perspective to the marketplace, creating real advantages for customers and wearers. For more information, visit www.coopervision.com. Job Summary Support key functions at the CooperVision Henrietta Facility within the Quality Engineering team in Packaging and Distribution. Responsibilities include root cause investigation of NCRs and customer complaints, engineering change orders, validation, and risk management. Use Quality Engineering principles (Lean, Six Sigma, Problem Solving, Root Cause Analysis) to develop and optimize systems aligned with company strategy and quality standards. Responsibilities Establish sampling plans, develop quality plans, conduct FMEA activities, support reliability engineering, audits, and specification development. Investigate nonconformance, determine root cause, implement corrective and preventive actions, and evaluate their effectiveness. Analyze data for improvement opportunities, design experiments (DOE), and develop validation plans. Lead quality improvement projects, provide statistical support, and develop process performance criteria. Support audits, oversee process and product validations, and maintain documentation including risk management files and quality records. Partner with Quality Assurance to oversee systems, deliver training, and provide process mapping and guidance. Qualifications Project management and problem-solving skills, communication and leadership abilities, experience with data analysis and statistical tools (Six Sigma GB/BB or CQE preferred). Knowledge of Quality System Regulations (21 CFR PART 820, ISO 13485), proficiency in Microsoft Office, Minitab; familiarity with BAAN, Agile, JDA is a plus. Work Environment Normal office environment, ability to perform physical work, potential travel. Experience Minimum 3+ years in medical device distribution and packaging operations or equivalent. Education Bachelor’s degree in engineering or related field; certification such as CQE, Green Belt, or Lean preferred. We are committed to equal employment opportunity. Salary range for U.S. locations: $68,900 - $91,867 per year, with potential benefits and other compensation. Seniority level
Mid-Senior level Employment type
Full-time Job function
Quality Assurance Industries
Medical Equipment Manufacturing
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Quality Engineer
role at
CooperVision Direct message the job poster from CooperVision Job Description CooperVision, a division of CooperCompanies (NASDAQ:COO), is one of the world’s leading manufacturers of soft contact lenses. The Company produces a full array of daily disposable, two-week and monthly contact lenses, all featuring advanced materials and optics. CooperVision has a strong heritage of solving the toughest vision challenges such as astigmatism, presbyopia and childhood myopia; and offers the most complete collection of spherical, toric and multifocal products available. Through a combination of innovative products and focused practitioner support, the company brings a refreshing perspective to the marketplace, creating real advantages for customers and wearers. For more information, visit www.coopervision.com. Job Summary Support key functions at the CooperVision Henrietta Facility within the Quality Engineering team in Packaging and Distribution. Responsibilities include root cause investigation of NCRs and customer complaints, engineering change orders, validation, and risk management. Use Quality Engineering principles (Lean, Six Sigma, Problem Solving, Root Cause Analysis) to develop and optimize systems aligned with company strategy and quality standards. Responsibilities Establish sampling plans, develop quality plans, conduct FMEA activities, support reliability engineering, audits, and specification development. Investigate nonconformance, determine root cause, implement corrective and preventive actions, and evaluate their effectiveness. Analyze data for improvement opportunities, design experiments (DOE), and develop validation plans. Lead quality improvement projects, provide statistical support, and develop process performance criteria. Support audits, oversee process and product validations, and maintain documentation including risk management files and quality records. Partner with Quality Assurance to oversee systems, deliver training, and provide process mapping and guidance. Qualifications Project management and problem-solving skills, communication and leadership abilities, experience with data analysis and statistical tools (Six Sigma GB/BB or CQE preferred). Knowledge of Quality System Regulations (21 CFR PART 820, ISO 13485), proficiency in Microsoft Office, Minitab; familiarity with BAAN, Agile, JDA is a plus. Work Environment Normal office environment, ability to perform physical work, potential travel. Experience Minimum 3+ years in medical device distribution and packaging operations or equivalent. Education Bachelor’s degree in engineering or related field; certification such as CQE, Green Belt, or Lean preferred. We are committed to equal employment opportunity. Salary range for U.S. locations: $68,900 - $91,867 per year, with potential benefits and other compensation. Seniority level
Mid-Senior level Employment type
Full-time Job function
Quality Assurance Industries
Medical Equipment Manufacturing
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