Automation Engineer
Systellar Technologies - keene, NH
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Automation Engineer Keene, New Hampshire Engagement Overview: Primary work location = Keene, NH. Occasional travel to Cambridge, Ontario and Southington, CT will be required. Workload: Two manufacturing equipment systems in development for Southington, CT facility. Supported by Keene personnel. High speed automation line from supplier in Canada. Industrial batch washing/siliconization system from supplier in Italy. Automation equipment being transferred from Keene. ~ 15 high output automation assembly lines. Production support to Keene Operations team Responsibilities Support design reviews, debug, acceptance and validation activities for equipment being developed by external suppliers. Support decommissioning of equipment at Keene site and recommissioning at Southington site. Support Keene production as needed Estimated duration: 6 to 9 months Candidate level: Engineer at E2, E3 or Senior. Open to principal level. Qualifications: 4+ years' experience in a medical device manufacturing environment. Validation experience: IQ, OQ, PQ and TMVs Automation control systems background - PLCs, HMI, Servos & Robots. Familiarity with standard MS Office tools. Good verbal and written communication skills. Additional desired qualifications - not mandatory: Fundamental knowledge of statistical analysis - specifically GR&Rs & Process Capability. Allen-Bradley programming experience. ______________________________________________________________________________________________________ Process Engineer Job Description Keene, New Hampshire Engagement Overview: Primary work location = Keene, NH. Occasional travel to and Southington, CT will be required. Workload: Two manufacturing equipment systems in development for Southington, CT facility. Supported by Keene personnel. High speed automation line from supplier in Canada. Industrial batch washing/siliconization system from supplier in Italy. Automation equipment being transferred from Keene. ~ 15 high output automation assembly lines. Production support to Keene Operations team Responsibilities Develop new process for siliconization of syringe plunger tips Experiments with legacy equipment to justify elimination of bonding agent and define process output requirements. Design verification samples. Development of process for new equipment. Validation of new equipment and process. Support Keene production with sustaining project execution. Support design reviews, debug, acceptance and validation activities for equipment being developed by external suppliers. Estimated duration: 6 to 9 months Candidate level: Engineer at E2, E3 or Senior. Open to principal level. Qualifications: 4+ years' experience in a medical device manufacturing environment. Process development experience. Validation experience: IQ, OQ, PQ and TMVs Strong background in statistical methods: DOEs, GR&Rs & Process Capability. Familiarity with standard MS Office tools. Good verbal and written communication skills. Additional desired qualifications - not mandatory: Familiarity with automation assembly systems Have a Great Day !!! Regards, Mandy EMAIL: Phone : + TextNow : +
Created: 2024-10-17