Manufacturing Visual Inspection

We are looking for Manufacturing Visual Inspection for our client in Fremont, CA.

Job Title: Manufacturing Visual Inspection

Job Location: Fremont, CA

Job Type: Contract

Job Overview:

Pay Range: $22.80hr - $27.80hr

Requirement/Must Have:

• 1+ years of experience in cGMP regulated industry.
• 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.

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 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: Logistics Coordination, Batch record executions, Equipment use logs, 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.

Education and Experience:

• High school degree + minimum 1 year work experience in GMP regulated industry.
• Associates/Bachelor s degree or biotechnology vocational training preferred.