Posted:2 days ago|
Platform:
On-site
Full Time
The responsibilities include handling a team of 45 subordinates, distributing job descriptions, and formulating and implementing SOPs. Key duties involve line clearance activities, cross-verifying stereo received at site, and managing retail samples. The role covers in-process quality assurance of all types of drugs and dosage forms, supervision of primary packing, and ensuring compliance with quality standards. It also involves issuing and reviewing log sheets, logbooks, and QMS forms. Additional responsibilities include synchronizing product manufacturing processes and verifying finished goods transfer tickets during dispatch to ensure accuracy, traceability, and compliance with regulatory and organizational requirements.
ZEON BIOTECH PRIVATE LIMITED
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