• Primary work location = Keene, NH. Occasional travel to Southington, CT will be required.
• Workload:
o Two manufacturing equipment systems in development for Southington, CT facility.
§ Supported by Keene personnel.
§ High speed assembly automation line from supplier in Canada. Assembly of blood gas sample and syringe products.
§ Industrial batch washing/siliconization system from supplier in Italy.
o Automation equipment being transferred from Keene.
§ ~ 15 high output automation lines assembling discrete components (syringe & blood gas sample products).
o 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.
Candidate level:
• Engineer at E2, E3 or Senior. Open to principal level.
Qualifications:
• 4+ years’ experience in a medical device manufacturing environment.
• Strong preference for assembly automation systems experience.
• Validation experience: IQ, OQ, PQ and TMVs
• Automation control systems background – PLCs, HMIs, Vision systems, Servos & Robots.
• Familiarity with standard MS Office tools.
• Good verbal and written communication skills