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You will be updated with latest job alerts via emailIn process activity in production and packing area
Perform Line clearances activities as per defined instruction in SOP
Continuous monitoring of GMP and cGMP compliance at shop floor
Perform calibration of IPQA instrument on time.
Issuance review and control the change management activities i.e. implementation post implementation review and proof verification.
Calibration of IPQA instrument
MFR and review the MBR in MES
Review of various protocol & reports related to Equipment Qualification Process validation Hold Time Miscellaneous & Cleaning Validation activities
Required Experience:
Senior IC
Full-Time