Diagnostic Oligo Manufacturing Technician I/II/III - Swing Shift

Posted on Sep 27, 2024 by LGC Biosearch Technologies
Petaluma, CA
Manufacturing
Immediate Start
Annual Salary
Full-Time
Job Description

The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management.

Swing Shift: Monday-Thursday, 4 x 10 hours, 1300-2330 (PetDx)

Essential Functions:

Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director.

Maintain batch records, equipment logs and other production records as directed per company procedures.

Follow current Good Manufacturing Practices (cGMP) and close adherence to internal SOPs utilizing GDP practices.

Perform routine operation, maintenance, inspection and cleaning of equipment in accordance with operational instructions

Quick and effective diagnosis of routine problems in manufacturing steps

Initiate attention to operators and tag-outs per documented processes

Execute Deviation and Nonconformance action plans

Reporting of safety incidents or safety hazards to senior colleagues, supervisors or managers

Maintain a clean an orderly laboratory environment.

Reference: 202576738

https://jobs.careeraddict.com/post/95610930

Diagnostic Oligo Manufacturing Technician I/II/III - Swing Shift

Posted on Sep 27, 2024 by LGC Biosearch Technologies

Petaluma, CA
Manufacturing
Immediate Start
Annual Salary
Full-Time
Job Description

The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management.

Swing Shift: Monday-Thursday, 4 x 10 hours, 1300-2330 (PetDx)

Essential Functions:

Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director.

Maintain batch records, equipment logs and other production records as directed per company procedures.

Follow current Good Manufacturing Practices (cGMP) and close adherence to internal SOPs utilizing GDP practices.

Perform routine operation, maintenance, inspection and cleaning of equipment in accordance with operational instructions

Quick and effective diagnosis of routine problems in manufacturing steps

Initiate attention to operators and tag-outs per documented processes

Execute Deviation and Nonconformance action plans

Reporting of safety incidents or safety hazards to senior colleagues, supervisors or managers

Maintain a clean an orderly laboratory environment.

Reference: 202576738

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