Manufacturing Visual Inspection Technician

Job Title: Manufacturing Visual Inspection Technician

Job Location: Fremont, CA

Job Type: Contract

Pay Range: $22.79hr - $27.79hr

Job Overview:

The Manufacturing Visual Inspection Technician executes routine unit operations in Visual Inspection as assigned, related to the manufacturing of drug products in a multi-product facility. The candidate will perform duties under limited supervision and according to standard operating and manufacturing procedures, supporting quality activities, packaging, and logistics operations.

Responsibilities:

• 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, advance visual inspection, palletizing, 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 including Logistics Coordination, Batch record executions, Equipment use logs, Work order initiation and tracking, Support Projects, and 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 personal 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:

• 1+ years of experience in a 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.

Education:

• High school diploma + minimum 1+ years of work experience in a GMP-regulated industry.
• Associate s/Bachelor s degree or biotechnology vocational training preferred.

Physical Requirements(Due to nature of job, The candidate must have):

• Ability to clear vision testing (acuity and color blindness).
• Ability to exert physical effort.
• Ability to lift up to 25 lbs.

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• Medical, Dental, and Vision Insurance
• 401(k) Retirement Plan
• Health Savings Account (HSA)
• Disability Insurance (Short-Term and Long-Term)
• Life and AD&D Insurance
• Paid Sick Leave (where required by applicable state or local law)
• Supplemental Insurance Plans
• Identity Theft Protection
• Pet Insurance
• Employee Wellness Programs
• Employee Assistance Program (EAP)
• Career Growth and Professional Development Opportunities