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Bachelor’s degree in Engineering, Quality, Manufacturing, Industrial Engineering, or a related technical field.
Minimum 4 years of experience in Quality Engineering, Manufacturing Engineering, New Product Introduction, or Process Validation within a regulated industry.
Experience applying process validation principles in accordance with FDA Quality System Regulation and ISO standards.
Fluent English and Spanish (written and spoken).
Experience with Production Part Approval Process (PPAP), risk management methodologies, and supplier quality activities.
Experience using statistical tools and methods, including hypothesis testing, process capability analysis, design of experiments (DOE), and data interpretation.
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Experience supporting sterilization validation and sterile packaging processes.
Experience working with manufacturing transfers, design transfer activities, and medical device quality systems.
Puerto Rico: $69,500 - $110,900 USD Annual
Stryker is a global medical technology company offering innovative products and services in surgical equipment, neurotechnology, orthopaedics, and spine care.
Visit company websiteJobs and hiring trendsUSD 69500-110900 / year
Temporary
Senior · 4+ years experience
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