Hope you are doing great!!
This is Akash from Solve IT. Please review the requirement below and share the updated resume, including the candidateās work authorization and rate expectation
Please Share resumes atĀ ak...@solveitservicesinc.com
LinkedIn IDĀ -Ā linkedin.com/in/akash-goyal-4470551a0
šØĀ We Are Hiring ā Validation Engineer SupportĀ šØ
šĀ Location: North Haven, CT
ā³Ā Duration: 12 Months
We are actively looking for experienced Validation Engineers with prior Medtronic experience to support a high-impact manufacturing and validation initiative for surgical device production.
šĀ Eligibility:
āĀ Prior Medtronic experience (Mandatory)
āĀ Work Authorization: H1B / GC / USC
š¼Ā Key Responsibilities:
⢠Oversee and optimize complex production processes for surgical devices, ensuring efficiency and quality standards.
⢠Act as the technical expert for electro-mechanical equipment, performing root cause analysis and implementing corrective actions.
⢠Lead process validation activities (IQ/OQ/PQ) for new and existing manufacturing equipment.
⢠Apply Lean manufacturing principles to improve process stability and reduce waste.
⢠Lead NCMR and CAPA investigations to maintain quality compliance.
⢠Support adaptation of machine/equipment design to production environments.
šÆĀ Required Qualifications:
⢠Bachelorās degree in Electrical Engineering, Automation, Controls, Mechatronics, or related field.
⢠10+ years of manufacturing engineering experience (or 8+ with a Masterās).
⢠Strong expertise in Medical Device Process Validation (IQ/OQ/PQ).
⢠Experience with Minitab, statistical analysis, DOE, process capability & control.
⢠Hands-on troubleshooting of automation systems, robotics, motion control, and machine vision.
⢠Strong knowledge of PPAP for component qualification.