Job Description

Job Summary

Supports the production of pharmaceutical products according to schedule through the maintenance of the clean room environment and associated records to comply with regulatory requirements, current good manufacturing practices (cGMP), and standard operating procedures.


Responsibilities


Reasonable accommodation will be made to enable individuals with disabilities to perform the essential functions.

  • Follow all written procedures according to GMP standards.
  • Operate and maintain non-viable particulate (NVP) machine and SAS air sampler and perform Viable sampling using contact plates for cleanrooms.

  • Perform Protocol execution for various validation studies for cleanroom areas and equipment.

  • Use Lab Vantage LIMS for all routine and non-routine sampling processes (sample collection and submission to labs).

  • Perform compressed gas sampling using MAS-100 unit (portable air sampler...

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