Posted:9 hours ago|
Platform:
Work from Office
Full Time
Responsible for all in process Quality Assurance Activities
Document issuance and control
Preparation and review of SOPs, Protocols, Reports, BMR, BPR and QC Specifications
Issuance and review of BMR and BPR and other quality system documents
Internal audit and its compliance related activity
Ensuring compliance to cGMP
Prepare Annual Training Plan in co-ordination with Head of QA
Schedule and coordinate the cGMP training session
Assist in the delivery of new employee orientation training
Assure training records are maintained for regular, temporary and contractors/consultants
Check monthly log book and calibration of IPQA instrument and balance
Stability and control sample management
Should be worked in QA Department
Well versed with computers, MS officer knowledge is must.
documentation skills required
Lok-beta Pharmaceuticals
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