Job Description

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 Details Responsibilities Achieve cost savings by implementing cost reduction projects like cycle time improvement, jigs and fixtures, process automation, spare parts consolidation, defect reduction, etc. Direct, communicate, and manage projects including but not limited to design and engineering improvement of assembly processes, bonding, plastic welding, sealing, cutting, printing, coiling, leak testing, etc. Ensure each equipment, jigs and fixtures and tooling is up-to-date per equipment/ tooling master list and the respective drawings. Ensure all preventive maintenance and calibration requirements are fulfilled for all equipment and tooling. Integrate and align efforts from different sources by directing, supervising and/ or otherwise managing project team members and/ or contractors as required for successful CI project completion. Maintain production by supporting new products, processes, transfers, and existing production. Prepare annual repair and maintenance budget. Prepare documentation by writing and redacting scope of work, business case, user requirements, request for quotation, validation protocol and report. Provide any combination of equipment/ tools and component attributes to various functions within the organization for decision making processes. Provide, measure, monitor and analyze maintenance and engineering activities - leading the local computerized maintenance management system (CMMS) deployment. Research, investigate, test, and develop product transfer technology including manufacturing and testing equipment; and provides hands on troubleshooting to the mentioned technology. Comply with the ISO14001 Environmental Management System policy, SOP and requirements Continuous support to the development and implementation of program to achieve and maintain the ISO 14001 environmental management system. Performs other tasks as required. Job Requirement 3+ years of experience with a Bachelor\'s degree in Engineering, life Science or equivalent Experience in years as specified above in stability/shelf-life studies development, planning, execution and documentation. Preferred: Experience with in Medical Device, pharmaceutical industrial. Experience in manufacturing process control and process validation requirements, including statistical tools EEO Policy Statement -

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