Visual Inspection Technician – GMP Manufacturing

Planet Pharma

Fremont (CA)

In loco

USD 30.000 - 39.000

Tempo pieno

4 giorni fa
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Generatore di candidature

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Descrizione del lavoro

Planet Pharma is seeking a detail-oriented technician for visual inspection and related duties in a multi-product manufacturing facility in Fremont, CA. You will perform routine unit operations, support drug product filling and packaging, and maintain 5S standards with adherence to cGMP/SOPs.

The role requires strong communication, ability to work with MES, and team collaboration in a fast-paced environment. Associates or Bachelor’s degree preferred; HS diploma with 1+ year experience acceptable.

Competenze

  • 1+ years of experience in a cGMP regulated industry.
  • Ability to concentrate on detail-oriented work in a complex technical environment.
  • Strong written and verbal communication skills.
  • Ability to work with computer-based systems and MES.
  • Ability to read and understand SOPs and document work per cGMP standards.
  • Ability to work as part of a high-performing team.

Mansioni

  • Executes routine unit operations in Visual Inspection as assigned.
  • Performs internal support duties including assisting drug product filling and packaging.
  • Maintains production areas according to predefined standards (5S).
  • Reports abnormalities and deviations in a timely and accurate manner.
  • Adheres to safety standards and escalates unsafe situations.
  • Contributes to Quality investigations and corrective actions.

Conoscenze

Detail-oriented
cGMP experience
Strong communication
MES experience
SOP comprehension
Team collaboration
Visual inspection

Formazione

High school diploma
Associates/Bachelor’s preferred

Strumenti

MES

Descrizione del lavoro

Planet Pharma is seeking a detail-oriented technician for visual inspection and related duties in a multi-product manufacturing facility in Fremont, CA. You will perform routine unit operations, support drug product filling and packaging, and maintain 5S standards with adherence to cGMP/SOPs.

The role requires strong communication, ability to work with MES, and team collaboration in a fast-paced environment. Associates or Bachelor’s degree preferred; HS diploma with 1+ year experience acceptable.

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