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Manufacturing Visual Inspection

Sigma Inc

Fremont, CA

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JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Cleanroom, Communication Skills, Computer Skills, Continuous Improvement, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Current Good Manufacturing Practice (cGMP), Detail Oriented, Documentation, Drug Manufacturing, Drug Products, High School Diploma, Lift/Move 25 Pounds, Maintain Compliance, Manufacturing, Manufacturing Execution Systems (MES), Manufacturing Operations, Mentoring, Operational Improvement, Pallet Jack, Presentation/Verbal Skills, Product Support, Production Support, Project Tracking, Quality Assurance, Quality Metrics, Regulations, Regulatory Requirements, Safety Training, Standard Operating Procedures (SOP), Writing Skills
LOCATION
Fremont, CA
POSTED
Today

37457636 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

About the Company

S

Sigma Inc

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