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Perform environmental monitoring in cleanroom environments.
Operate EM equipment such as Solairs, ApexZ50, and active counters.
Document results in compliance with GMP standards.
Prepare buffers and components; operate autoclaves.
Assist with cleanroom setup and stocking.
Support aseptic processing activities.
Complete and maintain batch records and EM forms.
Ensure adherence to GMP production protocols.
Participate in initial training and shift assignments.
Utilize Microsoft Office for recordkeeping and documentation tasks.
Mid-Senior level
Contract
Quality Assurance, Manufacturing, and Research
Biotechnology Research and Pharmaceutical Manufacturing