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Manufacturing Visual Inspection (2nd shift)

Aequor


Job Location:

Fremont, CA - USA

Monthly Salary: Not provided by the employer
Posted: 23 October 2026 (12 hours ago)
Application Deadline: 20 January 2027
Vacancies: 1 Vacancy

Job Summary

Duties:

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.



Skills:

-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.

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.

NOTE: Worker required to clear VISION TESTING (acuity & color blindness) before starting assignment.



Education:

  • High school degree minimum 1 year work experience in GMP regulated industry

  • Associates/Bachelors degree or biotechnology vocational training preferred


Schedule Notes:2nd Shift: Mon-Fri 2PM-10:30PM


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