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.
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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 : +1 201 855 5604
TextNow : +1 732 398 5499
linkedin.com/in/manender-singh-24aa2894