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2nd Shift Manufacturing Visual Inspection


Job Location:

Fremont, CA - USA

Monthly Salary: Not provided by the employer
Posted: 20 September 2026 (6 hours ago)
Application Deadline: 18 December 2026
Vacancies: 1 Vacancy

Job Summary

Manufacturing Visual Inspection Technician 2nd Shift Fremont CA 12 Month Contract

Location: Fremont CA
Industry: Pharmaceutical / Biotechnology Manufacturing
Shift: 2nd Shift (MondayFriday
2PM-10:30PM)
Duration: 12 Months Contract
Work Type: Onsite

About the Role

Sigma Inc is seeking a detail-oriented Manufacturing Visual Inspection Technician to support drug product manufacturing operations in a cGMP-regulated multi-product pharmaceutical facility.

This role focuses on visual inspection quality assurance and production support ensuring products meet strict regulatory and quality standards.

Key Responsibilities
  • Perform visual inspection and advanced visual inspection of drug products
  • Execute palletizing cleaning and inspection hood preparation
  • Support drug product filling and packaging operations
  • Operate within BioMES / Manufacturing Execution Systems (MES)
  • Complete batch record documentation and equipment logs
  • Initiate and track work orders and production activities
  • Maintain compliance with cGMP and cGDP standards
  • Identify report and document deviations abnormalities and quality issues
  • Participate in quality investigations and corrective actions (CAPA)
  • Maintain cleanroom standards (5S practices)
  • Assist in training and mentoring team members
  • Support continuous improvement and operational excellence initiatives
Additional Duties
  • Follow Standard Operating Procedures (SOPs) and manufacturing guidelines
  • Maintain accurate documentation for compliance and audits
  • Collaborate with cross-functional teams in a high-performance environment
  • Adhere to all safety and regulatory requirements
Requirements

Required:

  • High School Diploma or GED
  • Minimum 1 year experience in a cGMP-regulated environment
  • Strong attention to detail and quality-first mindset (Right First Time)
  • Experience with visual inspection or manufacturing operations
  • Ability to read and follow SOPs and work instructions
  • Basic computer skills and experience with MES systems
  • Strong written and verbal communication skills

Preferred:

  • Associate or Bachelors degree (Biotechnology or related field)
  • Experience in pharmaceutical or biotech manufacturing
  • Familiarity with batch records deviation reporting and quality systems
Physical & Work Requirements
  • Must pass vision testing (including color vision)
  • Ability to perform detail-oriented visual work for extended periods
  • Capable of lifting up to 25 lbs
  • Comfortable working in a cleanroom / controlled environment