Manufacturing Technician

Infotree Global Solutions; Sunnyvale (CA); On-site; USD 52,000 - 78,000; Full time

Job summary

Infotree Global Solutions is seeking a manufacturing operator to execute daily production activities aligned with the schedule, procedures, and quality standards. You will operate both manual and automated equipment, maintain records, and ensure GMP, SOP, GDP compliance.

The role requires 1–2 years in manufacturing, familiarity with pharmaceutical or medical device environments, and strong communication and teamwork skills to ensure safe, efficient operations.

Qualifications

• High School Diploma or equivalent.
• 1–2 years in a manufacturing environment.
• Experience in pharmaceutical, biotechnology, or medical device manufacturing preferred.
• Basic knowledge of GMP, SOPs, and GDP.
• Good communication, teamwork, and attention to detail.

Responsibilities

• Execute daily production schedules, including product changeovers, in-process reviews, and packaging activities.
• Operate manual and automated manufacturing equipment as per approved procedures.
• Follow SOPs, GMP requirements, and GDP.
• Maintain accurate production records and batch documentation.
• Perform equipment setup, cleaning, and routine checks.
• Ensure compliance with quality, safety, and housekeeping standards.
• Report equipment issues, process deviations, and quality concerns to the supervisor.
• Coordinate with production and quality teams to ensure smooth operations.

Skills

Good communication

Teamwork

Attention to detail

Education

High School Diploma

Job description

Responsible for executing daily manufacturing and production activities in accordance with the production schedule, approved procedures, and quality standards. The role involves operating manual and automated equipment while ensuring compliance with GMP, SOPs, and Good Documentation Practices (GDP).

Key Responsibilities

• Execute daily production schedules, including product changeovers, in-process reviews, and packaging activities.
• Operate manual and automated manufacturing equipment as per approved procedures.
• Follow SOPs, GMP requirements, and Good Documentation Practices.
• Maintain accurate production records and batch documentation.
• Perform equipment setup, cleaning, and routine checks.
• Ensure compliance with quality, safety, and housekeeping standards.
• Report equipment issues, process deviations, and quality concerns to the supervisor.
• Coordinate with production and quality teams to ensure smooth operations.

Qualifications & Experience

• High School Diploma
• 1-2 years of experience in a manufacturing environment.
• Experience in pharmaceutical, biotechnology, or medical device manufacturing is preferred.
• Basic knowledge of GMP, SOPs, and GDP.
• Good communication, teamwork, and attention to detail.