We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.
Job DetailsAssure laboratory receives documentation required to initiate testing and review of laboratory test reports for acceptability.
• Compile all disposables Product History documentation in preparation for submission to QS, ensuring information is present, accurate and meets all GMP requirements.
• Compile, process, and analyze Quality data under the direction of the Manufacturing Department, in support of all manufacturing activities, in the investigation of potential and actual quality defects, and in the development of corrective actions.
• Maintain filing of all master documents.
• Maintain manufacturing databases, as well as the manual filing system for cleaning records and other quality records.
• May edit documentation manuals to adhere to SOPs (Standard Operating Procedures) and GMPs (Good Manufacturing Practices).
• Perform analysis of data charts. • Prepare certifications for supervisor’s signatures.
• Prepare monthly charts and graphs for Manufacturing.
• Provide direction, training and support to manufacturing group.
• Review Disposable Device History Records and sub-assemblies for completeness.
• Support all aspects of inventory control including cycle counts, inventory adjustments and physical inventory.
High School diploma or equivalent required
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What We Do
Haemonetics (NYSE: HAE) is a global healthcare company dedicated to providing a suite of innovative medical products and solutions for customers, to help them improve patient care and reduce the cost of healthcare. Our technology addresses important medical markets: blood and plasma component collection, the surgical suite, and hospital transfusion services. To learn more about Haemonetics, visit www.haemonetics.com.
