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Manufacturing Visual Inspection

Fladger Associates
Fremont, CA Full Time
POSTED ON 3/8/2025
AVAILABLE BEFORE 6/7/2025

Fremont, CA

Contract Duration : 6-36 months

Rate : Negotiable

Responsibilities :

  • Excellent employment opportunity for a Manufacturing Visual Inspection in the Fremont, CA area.
  • 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 as visual inspection, advance 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 :
  • 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 and 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.

Experience :

  • High School Diploma minimum 1 year work experience in GMP regulated industry
  • Associates / Bachelor's degree or biotechnology vocational training preferred1 or more years of experience in 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.
  • PHYSICAL DEMANDS :
  • Duties of this position may require the incumbent to exert some physical effort.

  • Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds.
  • Employees required to participate and have acceptable result from vision testing including color blindness.
  • Schedule : 2nd Shift : Monday-Friday, 2 : 00PM to 10 : 30PM
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