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.
Assure 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 supervisors 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
Haemonetics provides a suite of innovative medical technology solutions that improve the quality, effectiveness and efficiency of care. We challenge ourselves to think big and make new possibilities a reality, so that our customers can make it matter for patients, every single day..