Posted:Just now|
Platform:
Work from Office
Full Time
1. Preparation of Annual/Periodic Product Quality Review (APQR/PQR) 2. Preparation of finished product specification (Tablet, External preparations & Injection) 3. Preparation of Protocol and Reports of PROCESS VALIDATION Batches. 4. Handling of Incidents, Deviation, CCP, OOS, OOT and Material Rejections 5. Issuing BARCODES for new Registered products in coordination with regulatory department. 6. Working Hands on MARKET COMPLAINTS and CAPA. 7. Preparation of Master Formula Record (MFR) and Preparation Of (SOPs). 8. Preparation of EQUIPMENT QUALIFICATION documents i.e. IQ, OQ, PQ protocol and Reports during Installation of New Instruments/ Equipments. 9. Identification of Hazard and Calculation of Risk associated with product or daily activity. 10 Participation and Handling of SELF INSPECTION Reports (INTERNAL AUDIT). 11. Preparation of Audit & Maintenance of Post Audit Documents (compliance reports). Desired Candidate Profile Bachelor's degree in Science (B.Sc) or Pharmacy (B.Pharma). Male candidate will be preferred.
Nem Laboratories
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