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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
1 day ago

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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