Manufacturing Technician

Infotree Global Solutions; Santa Clara (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

Infotree Global Solutions is seeking a skilled Manufacturing Technician to support production and assembly of medical devices in a regulated environment. The role emphasizes hands-on manufacturing, adherence to SOPs, and strict documentation.

You will perform assembly, inspect, test, package, and operate tools safely, maintain cleanroom standards when applicable, and help ensure GMP/ISO 13485 compliance. This position requires 1–3 years in manufacturing, a high school diploma or GED, and the

Qualifications

• 1–3+ years of manufacturing or production experience, preferably in medical devices or another regulated industry.
• High school diploma or GED; technical education or certification is a plus.
• Experience following SOPs, work instructions, drawings, or detailed manufacturing specifications.
• Ability to stand for extended periods and perform repetitive assembly tasks.

Responsibilities

• Perform assembly, manufacturing, inspection, testing, and packaging activities according to approved SOPs and work instructions.
• Operate manufacturing tools, equipment, and fixtures safely and efficiently.
• Complete production records, device history records, and other required documentation accurately.
• Follow GMP, ISO, and company quality procedures and maintain compliance with applicable regulations.
• Perform in-process inspections and identify product defects or manufacturing issues.
• Troubleshoot routine equipment and process problems and elevate issues when necessary.
• Maintain a clean, organized, and safe work environment, including following cleanroom procedures when applicable.

Skills

Attention to detail

Manufacturing experience

SOP adherence

Documentation

Education

High school diploma or GED

Technical education or certification

Job description

We are seeking a skilled and detail-oriented Manufacturing Technician to support the production and assembly of medical devices in a regulated manufacturing environment. The ideal candidate will have hands‑on manufacturing experience, preferably within the medical device, pharmaceutical, biotechnology, or other regulated industries.

Key Responsibilities

• Perform assembly, manufacturing, inspection, testing, and packaging activities according to approved SOPs and work instructions.
• Operate manufacturing tools, equipment, and fixtures safely and efficiently.
• Complete production records, device history records, and other required documentation accurately.
• Follow GMP, ISO, and company quality procedures and maintain compliance with applicable regulations.
• Perform in-process inspections and identify product defects or manufacturing issues.
• Troubleshoot routine equipment and process problems and elevate issues when necessary.
• Maintain a clean, organized, and safe work environment, including following cleanroom procedures when applicable.

Qualifications

• High school diploma or GED required; technical education or certification is a plus.
• 1–3+ years of manufacturing or production experience, preferably in medical devices or another regulated industry.
• Experience following SOPs, work instructions, drawings, or detailed manufacturing specifications.
• Ability to stand for extended periods and perform repetitive assembly tasks.

Preferred Experience

• Medical device manufacturing experience.
• Experience in an FDA-regulated and/or ISO 13485 environment.
• Knowledge of GMP, nonconformance, CAPA, and controlled documentation.
• Cleanroom or controlled-environment manufacturing experience.