Designer

HCL Technologies Limited; United States; On-site; USD 40,000 - 64,000; Full time

Job summary

HCL Technologies Limited is seeking technicians for intermediate electro-mechanical assembly of robotic system modules in a structured production line environment in the United States. You will build joints, control modules, and cable harnesses per engineering docs, and perform functional, electrical, and mechanical tests with calibrated tools.

Maintain compliance with ISO 13485, FDA QSR, and GDP; document outcomes in MES/ERP/SAP and electronic DHR systems; support NPI builds and continuous

Qualifications

• Perform intermediate electro-mechanical assembly of robotic modules per approved docs and work instructions.
• Meet daily build targets while maintaining ISO 13485, FDA QSR and GDP compliance.
• Interpret assembly procedures to correctly build mechanical and electromechanical components across product modules.
• Conduct functional, electrical, and mechanical tests with calibrated tools and fixtures.
• Identify and troubleshoot basic electrical and mechanical issues and escalate complex problems.
• Document production activities and test results following GDP.

Responsibilities

• Assemble robotic modules per engineering specs with minimal supervision.
• Maintain production line discipline to meet targets and quality standards.
• Run functional and electrical tests using calibrated equipment.
• Document results in MES/ERP and DHR systems per GDP.
• Provide feedback on processes and fixtures to support continuous improvement.
• Assist in training and mentoring entry-level technicians.

Skills

Electro-mechanical assembly

Quality compliance

Electrical testing

Troubleshooting

Documentation (GDP)

Tools

Test fixtures

Multimeters

ERP/SAP

Job description

Requisition ID184457-Posted10/26/2026

• Perform intermediate level electro‑mechanical assembly of robotic system modules including joints, control modules, and cable harnesses using engineering documentation and established work instructions with minimal supervision.
• Operate within a structured production line environment to meet daily build targets while maintaining compliance with ISO 13485, FDA QSR, and Good Documentation Practices (GDP).
• Interpret and apply defined assembly procedures to correctly build, verify, and validate mechanical and electromechanical components across multiple product modules.
• Conduct functional, electrical, and mechanical tests using calibrated tools, test fixtures, torque equipment, and multimeters.
• Identify, and troubleshoot basic electrical and mechanical issues (e.g., miswiring, misalignment, sensor faults) and upscale complex or systemic issues to engineering.
• Perform minor mechanical and electrical repairs to support production continuity, escalating complex issues to engineering.
• Maintain compliance with ESD controls, clean manufacturing protocols, and contamination‑control standards appropriate for medical device manufacturing.
• Accurately document production activities, test outcomes, and inspection data in MES, ERP/SAP, and electronic DHR systems following GDP.
• Perform in‑process inspections and contribute to quality verifications to ensure adherence to workmanship and regulatory standards.
• Assist in process updates by providing feedback on assembly sequences, documentation accuracy, and fixture/tool improvements.
• Support manufacturing engineering on the line setup, fixture validation, new product introduction (NPI) builds, and continuous improvement initiatives.
• Support training, knowledge‑sharing, and guidance for new or entry-level technicians
• Prepare production lines by performing line clearance, verifying equipment maintenance and calibration status, and ensuring material readiness—which includes accurate material transactions, cycle counts of raw materials, sub‑assemblies, and WIP, as well as proactively identifying and reporting shortages or discrepancies to prevent build interruptions and support efficient production scheduling.
• Maintain certification and demonstrate proficiency on at least three designated modules while meeting all safety, quality, and training requirements.

Key Responsibilities

Key Responsibilities

• Perform intermediate level electro‑mechanical assembly of robotic system modules including joints, control modules, and cable harnesses using engineering documentation and established work instructions with minimal supervision.
• Operate within a structured production line environment to meet daily build targets while maintaining compliance with ISO 13485, FDA QSR, and Good Documentation Practices (GDP).
• Interpret and apply defined assembly procedures to correctly build, verify, and validate mechanical and electromechanical components across multiple product modules.
• Conduct functional, electrical, and mechanical tests using calibrated tools, test fixtures, torque equipment, and multimeters.
• Identify, and troubleshoot basic electrical and mechanical issues (e.g., miswiring, misalignment, sensor faults) and upscale complex or systemic issues to engineering.
• Perform minor mechanical and electrical repairs to support production continuity, escalating complex issues to engineering.
• Maintain compliance with ESD controls, clean manufacturing protocols, and contamination‑control standards appropriate for medical device manufacturing.
• Accurately document production activities, test outcomes, and inspection data in MES, ERP/SAP, and electronic DHR systems following GDP.
• Perform in‑process inspections and contribute to quality verifications to ensure adherence to workmanship and regulatory standards.
• Assist in process updates by providing feedback on assembly sequences, documentation accuracy, and fixture/tool improvements.
• Support manufacturing engineering on the line setup, fixture validation, new product introduction (NPI) builds, and continuous improvement initiatives.
• Support training, knowledge‑sharing, and guidance for new or entry-level technicians
• Prepare production lines by performing line clearance, verifying equipment maintenance and calibration status, and ensuring material readiness—which includes accurate material transactions, cycle counts of raw materials, sub‑assemblies, and WIP, as well as proactively identifying and reporting shortages or discrepancies to prevent build interruptions and support efficient production scheduling.
• Maintain certification and demonstrate proficiency on at least three designated modules while meeting all safety, quality, and training requirements.

Skill Requirements

Key Responsibilities

• Perform intermediate level electro‑mechanical assembly of robotic system modules including joints, control modules, and cable harnesses using engineering documentation and established work instructions with minimal supervision.
• Operate within a structured production line environment to meet daily build targets while maintaining compliance with ISO 13485, FDA QSR, and Good Documentation Practices (GDP).
• Interpret and apply defined assembly procedures to correctly build, verify, and validate mechanical and electromechanical components across multiple product modules.
• Conduct functional, electrical, and mechanical tests using calibrated tools, test fixtures, torque equipment, and multimeters.
• Identify, and troubleshoot basic electrical and mechanical issues (e.g., miswiring, misalignment, sensor faults) and upscale complex or systemic issues to engineering.
• Perform minor mechanical and electrical repairs to support production continuity, escalating complex issues to engineering.
• Maintain compliance with ESD controls, clean manufacturing protocols, and contamination‑control standards appropriate for medical device manufacturing.
• Accurately document production activities, test outcomes, and inspection data in MES, ERP/SAP, and electronic DHR systems following GDP.
• Perform in‑process inspections and contribute to quality verifications to ensure adherence to workmanship and regulatory standards.
• Assist in process updates by providing feedback on assembly sequences, documentation accuracy, and fixture/tool improvements.
• Support manufacturing engineering on the line setup, fixture validation, new product introduction (NPI) builds, and continuous improvement initiatives.
• Support training, knowledge‑sharing, and guidance for new or entry-level technicians
• Prepare production lines by performing line clearance, verifying equipment maintenance and calibration status, and ensuring material readiness—which includes accurate material transactions, cycle counts of raw materials, sub‑assemblies, and WIP, as well as proactively identifying and reporting shortages or discrepancies to prevent build interruptions and support efficient production scheduling.
• Maintain certification and demonstrate proficiency on at least three designated modules while meeting all safety, quality, and training requirements.