Manufacturing Visual Inspection

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

Location: Fremont, CA Industry: Pharmaceutical / Biotechnology Manufacturing Shift: 2nd Shift (Monday–Friday, 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 Bachelor's 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