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Manufacturing Technician; Visual Inspection

Job in Fremont, Alameda County, California, 94537, USA
Listing for: Aequor
Full Time position
Listed on 2026-07-08
Job specializations:
  • Manufacturing / Production
    Production QC/QA, Pharmaceutical Manufacturing
  • Quality Assurance - QA/QC
    Production QC/QA
Salary/Wage Range or Industry Benchmark: 45000 - 60000 USD Yearly USD 45000.00 60000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Technician (Visual Inspection)

Job Title:

Manufacturing Visual Inspection

Contract Duration: 6-12 months

Location:

Fremont, CA

Duties
  • Executes routine unit operations in Visual Inspection as assigned related to the manufacturing of drug product in a multi-product facility.
  • Performs duties under limited supervision and according to standard operating and manufacturing procedures.
  • Executes independently with adequate training, complex fundamental operations such as:
  • Visual inspection
  • Advanced visual inspection
  • Cleaning
  • Inspection hood prep for operations
  • BioMES Operations and Exceptions
  • Performs internal support duties including assisting drug product filling and packaging.
  • Executes independently with adequate training fundamental operations:
  • Logistics Coordination
  • Batch record executions
  • Work order initiation and tracking
  • Support Projects
  • Support Creation/Maintain Training Kits
  • Documents work according to cGMP and cGDP.
  • Adheres to established regulations and follows cGMP established by site.
  • Reports abnormalities and deviations in a timely and accurate manner.
  • Adheres to safety standards and identifies unsafe situations/habits and escalates appropriately.
  • Maintains production areas according to predefined standards (5s).
  • Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification.
  • Contributes to Quality activities such as supporting investigations, corrective actions, and area walk-throughs.
Skills & Experience
  • 1 or more years of experience in cGMP regulated industry.
  • Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and “Right the first-time” mindset.
  • Strong written and verbal communication skills.
  • Ability to work with computer-based systems and manufacturing execution systems (MES).
  • Ability to read and understand SOPs and instructions and document work in a written format applying cGMP standards.
  • Ability to work as part of a high-performing team and collaborate effectively with staff.
  • Must be able to read and see clearly.
Physical Demands
  • Duties of this position may require the incumbent to exert some physical effort.
  • Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds.
  • Employees required to participate and have acceptable result from vision testing including color blindness.
Education
  • High school degree + minimum 1 year work experience in GMP regulated industry.
  • Associates/Bachelor's degree or biotechnology vocational training preferred.
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