Manufacturing Visual Inspection

TechMind RPO•Fremont, CA

8d•$15 - $20•Onsite

About The Position

This is an excellent employment opportunity for a Manufacturing Visual Inspection role in the Fremont, CA area. The position operates on the 2nd Shift, Monday through Friday, from 2:00 PM to 10:30 PM. The role involves executing routine unit operations in Visual Inspection related to drug product manufacturing in a multi-product facility. Duties are performed under limited supervision according to standard operating and manufacturing procedures. With adequate training, the incumbent will independently perform complex fundamental operations such as advanced visual inspection, palletizing, cleaning, inspection hood preparation, BioMES Operations, and handling exceptions. The role also includes internal support duties, such as assisting with drug product filling and packaging. Additionally, the position requires independent execution of fundamental operations including logistics coordination, batch record execution, equipment use logs, work order initiation and tracking, and supporting projects. The role also supports the creation and maintenance of training kits and documents work according to cGMP and cGDP standards. Adherence to established regulations and cGMP guidelines is mandatory. The incumbent will report abnormalities and deviations promptly and accurately, adhere to safety standards, and escalate any unsafe situations or habits. Maintaining production areas according to predefined 5s standards is also a key responsibility. The role requires maintaining personal training compliance and training other technicians and associates upon completion of trainer qualification. Contribution to Quality activities, such as supporting investigations, corrective actions, and area walk-throughs, is expected.

Requirements

High School Diploma + minimum 1 year work experience in GMP regulated industry
1 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.

Nice To Haves

Associates/Bachelor’s degree or biotechnology vocational training preferred

Responsibilities

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.