Visual Inspector

The Fountain Group; Fremont (CA); On-site; USD 32,000 - 45,000; Full time

Job summary

The Fountain Group is seeking a Visual Inspector for a Fremont, CA project. The position is a 6-month assignment onsite, with a start pay of $27.78 per hour.

The role focuses on routine unit operations in visual inspection for a multi-product pharmaceutical manufacturing facility. Work hours are Monday through Friday, 6:00am to 2:30pm PST, with adherence to cGMP and MES systems.

Qualifications

• High School Diploma or GED with 1 year of GMP experience.
• 1+ years of experience in a cGMP regulated environment.
• Experience with MES and computer-based systems.
• Ability to read SOPs and document work per cGMP standards.

Responsibilities

• Coordinate logistics for manufacturing operations.
• Execute batch records.
• Maintain equipment use logs.
• Initiate and track work orders.
• Support projects.
• Create/maintain training kits; document work per cGMP and cGDP.
• Follow site cGMP regulations.
• Report abnormalities and deviations promptly.
• Adhere to safety standards and escalate unsafe conditions.
• Maintain production areas in 5S condition.
• Maintain training compliance and train others after qualification.
• Contribute to quality investigations and corrective actions.

Skills

GMP experience

cGMP knowledge

Documentation

Attention to detail

Education

High School Diploma or GED with 1 year GMP experience

Tools

MES

Job description

We are a national staffing firm and are currently seeking a Visual Inspector for a prominent client of ours. This position is Fremont, CA 94555. Details of the position are as follows:

Job Details:

• Pay: $27.78/hr to Start!
• 6-month assignment, possibility for extension based on performance and budget.
• Monday-Friday: 6:00am-2:30pm PST. (Onsite)
• Position will be mainly responsible for executing routine unit operations in Visual Inspection related to the manufacturing drug product in a multi-product facility and perform duties under limited supervision according to standard operating and manufacturing procedures.
• Key Responsibilities:
  • 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, 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.

Qualifications:

• High School Diploma or GED with 1 year work experience in GMP regulated industry
• 1+ years of experience in cGMP regulated industry.
• 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.

Referral Bonus for any candidate who is hired and still gainfully employed after 30 days.

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