GMP Visual Inspection Technician

Planet Pharma

Fremont (CA)

On-site

USD 30,000 - 39,000

Full time

2 days ago
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Job summary

Planet Pharma is seeking a Visual Inspection Technician in Fremont, CA to execute routine unit operations in a multi-product manufacturing facility. You will perform visual inspection, palletizing, packaging support, and MES-related tasks under cGMP guidelines.

A detail‑oriented mindset and strong written/verbal communication are essential. The role requires 1+ year in a GMP environment, ability to follow SOPs, and collaboration within a high-performing team.

Qualifications

  • Minimum 1 year of experience in a cGMP-regulated environment.
  • Detail-oriented in a complex technical setting with a quality focus.
  • Strong written and verbal communication skills.
  • Experience with MES and computer-based manufacturing systems.
  • Ability to read SOPs and document work per cGMP.

Responsibilities

  • Perform routine unit operations in Visual Inspection per SOPs.
  • Support drug product filling and packaging.
  • Logistics coordination and batch record execution.
  • Operate equipment and log usage.
  • Prepare inspection hood and perform MES operations.
  • Contribute to quality investigations and corrective actions.
  • Ensure safety and 5S in production areas.
  • Train and mentor other technicians when qualified.

Skills

cGMP experience
Attention to detail
Verbal and written communication
MES systems
SOP comprehension
Team collaboration
Visual acuity

Education

Associates/Bachelor’s degree or biotechnology vocational training
High school diploma

Tools

MES (Manufacturing Execution System)
Computer-based systems

Job description

Planet Pharma is seeking a Visual Inspection Technician in Fremont, CA to execute routine unit operations in a multi-product manufacturing facility. You will perform visual inspection, palletizing, packaging support, and MES-related tasks under cGMP guidelines.

A detail‑oriented mindset and strong written/verbal communication are essential. The role requires 1+ year in a GMP environment, ability to follow SOPs, and collaboration within a high-performing team.

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