Manufacturing Technician II (2nd Shift)

Real Staffing; Santa Clara (CA); On-site; USD 34,000 - 48,000; Full time

Job summary

Real Staffing Group is seeking a Manufacturing Technician II for a surgical robotics production team in Santa Clara. You will perform electro-mechanical assembly, support schedules, and ensure compliance with medical device regulations in a fast-paced, regulated environment.

The role offers hands-on work with cutting-edge robotic technology, opportunities for growth, and collaboration with engineering and manufacturing teams on NPI and continuous improvement initiatives.

Qualifications

• 1–2 years of relevant manufacturing experience, or 3–4 years of experience in manufacturing or assembly within medical devices, electromechanical systems, robotics, or other regulated industries.
• Hands-on GDP in regulated manufacturing environments.
• Basic electrical troubleshooting with multimeters, grounding techniques and isolation methods.
• Proficiency with assembly tools such as torque wrenches, screwdrivers, calipers, presses, and multimeters.
• Ability to work overtime and weekends as business needs require.
• Strong written and verbal communication across multiple teams.
• Ability to manage multiple priorities in a fast-paced manufacturing environment.
• Ability to work independently as well as collaboratively within cross-functional teams.

Responsibilities

• Perform intermediate-level electro-mechanical assembly of robotic system modules, including joints, control modules, and cable harnesses, using engineering documentation and defined work instructions.
• Operate within a structured production line environment to meet daily build targets while maintaining ISO 13485, FDA QSR, and GDP compliance.
• Interpret and apply assembly procedures to build, verify, and validate components across product modules.
• Conduct functional, electrical, and mechanical tests using calibrated tools, fixtures, and measurement equipment.
• Identify and troubleshoot basic electrical/ mechanical issues; escalate complex problems to engineering.
• Maintain ESD controls, clean manufacturing protocols, and contamination control standards.
• Document production activities, test outcomes, and inspection data in MES, ERP/SAP, and DHR systems.
• Perform in-process inspections and contribute to quality verifications.
• Support manufacturing engineering activities including line setup, fixture validation, NPI builds, and continuous improvement.
• Assist training and knowledge sharing for new or entry-level technicians.
• Prepare production lines with line clearance, equipment calibration status, and material readiness; identify shortages.
• Maintain certification and demonstrate proficiency on at least three designated modules.

Skills

GDP

Electrical troubleshooting

Torque wrenches

Multimeters

Cross-functional collaboration

Communication

Time management

Education

Vocational certificate / technical degree / associate degree

Tools

SAP

MES

ComplianceWire

Job description

Manufacturing Technician II

Job Function

Supply Chain Manufacturing

Job Sub Function

Manufacturing Product & Packaging Operations

Job Category

Manufacturing Technician II

Location

Santa Clara, California

Position Summary

We are seeking a detail-oriented and experienced Manufacturing Technician II to join a dynamic surgical robotics production team. This role is responsible for performing electro-mechanical assembly of robotic modules and components, supporting production schedules, and maintaining compliance with medical device manufacturing regulations.

The ideal candidate can work independently, support both manufacturing and engineering activities, and thrive in a fast-paced, regulated production environment. This position provides hands-on experience with cutting-edge robotic technology and opportunities for long-term career growth.

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 Quality System Regulations (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 such as miswiring, misalignment, and sensor faults, escalating complex or systemic issues to engineering when necessary.
• 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 Device History Record (DHR) systems.
• Perform in-process inspections and contribute to quality verifications to ensure adherence to workmanship and regulatory standards.
• Support manufacturing engineering activities, including 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. This includes material transactions, cycle counts of raw materials, subassemblies, and work-in-process inventory, while proactively identifying shortages or discrepancies.
• Maintain certification and demonstrate proficiency on at least three designated modules while meeting all safety, quality, and training requirements.

Required Qualifications

• High school diploma or equivalent with:
  • 1-2 years of relevant manufacturing experience, or
  • 3-4 years of experience in manufacturing or assembly within medical devices, electromechanical systems, robotics, or other regulated industries.
• Hands-on experience with Good Documentation Practices (GDP) and regulated manufacturing environments.
• Basic electrical troubleshooting skills, including the use of multimeters, grounding techniques, and isolation methods.
• Proficiency with assembly tools such as torque wrenches, screwdrivers, calipers, presses, and multimeters.
• Ability to work overtime and weekends as business needs require.
• Strong written and verbal communication skills and the ability to work effectively across multiple teams.
• Ability to manage multiple priorities in a fast-paced manufacturing environment while maintaining accuracy and quality.
• Ability to work independently as well as collaboratively within cross-functional teams.

Preferred Qualifications

• Vocational certificate, technical degree, or associate degree with 2+ years of related experience.
• Experience working with Kanban systems, MES platforms, and software-based testing procedures.
• Experience using systems such as SAP, ComplianceWire, or similar manufacturing and quality systems.
• Exposure to robotics, surgical device manufacturing, or complex electromechanical assemblies.
• Experience troubleshooting robotic or automated systems.

Work Schedule

• Monday-Friday, 2:00 PM-10:30 PM (Onsite, Second Shift)
• Occasional weekend work may be required.
• Overtime may be required based on production demands - it will be paid out at time and a half.

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.