Posted:3 weeks ago|
Platform:
Work from Office
Full Time
Sampling, incubation, withdrawal, analysis of stability samples as per schedule.
Stability study monitoring as per requirements of regulatory authorities, vendor requirements and as per ICH guidelines. Submission of Stability testing form to PRC, RA, CFT and other department as per requirement.
Deviation logging, immediate action, impact assessment, investigation, root cause, remedial
action and closing within stipulated time in Trackwise (QMS) software
OOS, OOT, incidences and deviation
PLEASE SHARE YOUR UPDATED CV ON placement@balpharma.com
Thanks,
Kamal
Bal Pharma
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