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Manufacturing Technician

Sigma

2nd Shift Manufacturing Technician (Entry-Level, cGMP) – Fremont, CA | 6-Month Contract

Location: Fremont, CA (Onsite) Shift: 2nd Shift (Sun–Wed)

Sun–Tues: 3:00 PM – 1:30 AM

Wed: 3:00 PM – 11:30 PM Hours: 38 hours/week Duration: 4-Month Contract Company: Sigma Inc.

Job Overview

Sigma Inc. is hiring a Manufacturing Technician to support downstream biopharmaceutical manufacturing operations in a cGMP-regulated environment. This is an excellent entry-level opportunity for candidates interested in biotechnology, pharmaceuticals, or manufacturing careers.

You will perform hands-on production tasks, support equipment preparation, and ensure compliance with quality and safety standards in a fast-paced, team-oriented facility.

Key Responsibilities
  • Execute basic downstream manufacturing operations for bulk drug substance production
  • Perform weighing, dispensing, parts cleaning, and equipment setup
  • Support kit assembly, staging, and material handling
  • Assist with CIP (Clean-In-Place) and SIP (Sterilize-In-Place) processes (with supervision)
  • Prepare and transfer buffers and solutions
  • Maintain and clean manufacturing and analytical equipment
  • Stock materials, manage consumables, and discard expired reagents
  • Update and maintain controlled SOP documentation
  • Identify and report process deviations or equipment issues
  • Follow cGMP, cGDP, and safety compliance standards
  • Maintain clean and organized production areas using 5S principles
Required Qualifications
  • High School Diploma or equivalent
  • Ability to follow SOPs (Standard Operating Procedures) and work instructions
  • Strong attention to detail and "right-first-time" mindset
  • Basic computer skills and ability to document work accurately
  • Strong communication and teamwork skills
  • Willingness to work 2nd shift and flexible schedules in a 24/7 environment
Preferred Qualifications
  • Associate's or Bachelor's degree in Biotechnology, Life Sciences, or related field
  • 1+ year experience in a cGMP-regulated industry (pharma, biotech, or medical device)
  • Familiarity with:
    • Cleanroom environments
    • Manufacturing equipment
    • Quality and compliance standards
Vacancy posted 8 hours ago
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