Manufacturing Visual Inspection

Job Title: Manufacturing Visual Inspection

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 as assigned related to the manufacturing of drug products in a multi-product facility, performing duties under limited supervision according to standard operating and manufacturing procedures.

Responsibilities:

• Execute routine unit operations in visual inspection as assigned related to the manufacturing of drug products in a multi-product facility.
• Perform duties under limited supervision and according to standard operating and manufacturing procedures.
• Execute independently, with adequate training, complex fundamental operations such as visual inspection, advanced visual inspection, palletizing, cleaning, inspection hood preparation for operations, BioMES operations, and exceptions.
• Perform internal support duties including assisting with drug product filling and packaging.
• Execute 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/maintenance of training kits.
• Document work according to cGMP and cGDP standards.
• Adhere to established regulations and follow cGMP established by the site.
• Report abnormalities and deviations in a timely and accurate manner.
• Adhere to safety standards, identify unsafe situations/habits, and escalate appropriately.
• Maintain production areas according to predefined standards (5S).
• Maintain training compliance and train other technicians and associates on operations upon completion of trainer qualification.
• Contribute 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 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 a minimum of 1 year 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 exert physical effort.
• Ability to lift up to 25 pounds.

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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