Manufacturing Visual Inspection

Job Title: Manufacturing Visual Inspection

Job Location: Fremont, CA

Job Type: Contract

Job Overview:

Pay Range: $21.86hr - $26.86hr

Requirement/Must Have:

• 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 verbal and written 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.
• Worker required to clear VISION TESTING (acuity & color blindness) before starting assignment.

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 including Logistics Coordination, Batch record executions, and Equipment use logs.
• Handles work order initiation and tracking, support projects, and support creation/maintenance of training kits documents.
• 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 through.

Nice to Have:

• Associates/Bachelor s degree or biotechnology vocational training preferred.

Skills:

• CGMP Compliance.
• Visual Inspection.
• Advanced Visual Inspection.
• Palletizing.
• Cleaning.
• BioMES Operations.
• Logistics Coordination.
• Batch record executions.

Qualification And Education:

• High school degree + minimum 1+ years of work experience in a GMP-regulated industry.

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

• Ability to exert some physical effort.
• Ability to lift 25 pounds or more.

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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