Engagement Overview:
- Primary work location Keene NH. Occasional travel to Southington CT will be required.
- Workload:
- 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.
- Automation equipment being transferred from Keene.
- 15 high output automation lines assembling discrete components (syringe & blood gas sample products).
- 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.
Qualifications :
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.
Additional desired qualifications not mandatory:
- Fundamental knowledge of statistical analysis specifically GR&Rs & Process Capability.
- AllenBradley/Rockwell Automation programming experience: Studio5000 RSView ME/SE.
- Siemens S7 programming experience.
- Staubli/EPSON/ABB robot experience
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract