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 successful candidate will execute routine unit operations in visual inspection related to the manufacturing of drug products in a multi-product facility.

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, advanced 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 or maintenance of training kits.
• Documents work according to cGMP and cGDP standards.
• Adheres to established regulations and follows cGMP established by the site.
• Reports abnormalities and deviations in a timely and accurate manner.
• Adheres to safety standards, identifies unsafe situations or 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.
• Must be able to read and see clearly.

Education:

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

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

• 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