More jobs:
Manufacturing Technician
Job in
Santa Clara, Santa Clara County, California, 95053, USA
Listed on 2026-08-29
Listing for:
Infotree Global Solutions
Full Time
position Listed on 2026-08-29
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Production QC/QA, Production Associate / Production Line
Job Description & How to Apply Below
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.
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