Manufacturing Technician

Infotree Global Solutions; Santa Clara (CA); On-site; USD 52,000 - 76,000; Full time

Job summary

Infotree Global Solutions in California seeks a Manufacturing Technician to support the production and assembly of medical devices in a regulated environment. You will perform assembly, inspection, testing, and packaging per SOPs and work instructions, while maintaining accurate records.

The role demands standing for long periods and adherence to GMP/ISO quality procedures and cleanroom practices. Ideal candidates have 1–3+ years in manufacturing, medical device exposure, and the ability to

Qualifications

• High school diploma or GED; technical education or certification is a plus.
• 1–3+ years of manufacturing or production experience, preferably in medical devices or a regulated industry.
• 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 escalate issues when necessary.
• Maintain a clean, organized, and safe work environment, including following cleanroom procedures when applicable.

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 escalate 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.