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Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.

Post : Quality Analyst II

Job Description

IPQA Activity
• Sampling of In-process and finished products, which includes Process evaluation/validation samples in all the manufacturing stages as per requirement
• Performing In process checks during Manufacturing and Packaging
• Line clearances in Warehouse, Production and Packaging areas
• Collection of hold time study samples. Labelling of Raw/Packaging materials and in process/bulk finished product after approvals.
• Co-ordination with quality control personnel for sample handling. Collection of stability sample and reserve sample
• Review of IPQA related all log books

SAP R/3 System Handling :
• Release of Intermediate stage analytical reports of Tablets and capsules of commercial, validation, Pre-exhibit and Exhibit batches in SAP system
• Print additional pages of Batch Manufacturing Records and Batch Packaging Records
• Print Certificate of Analysis for In-process/Finished/Water/Stability etc. analytical reports in SAP system

Print Approved, Rejected Labels of Raw material, Packaging materials, in process and bulk finished product

Documentation
• Review of executed BMR and BPR
• Preparation and review of IPQA area related SOPs
• Preparation of Investigation report related to IPQA

Alert Investigations
• Preparation of Alert memo investigations
• Co-ordination with QC and Production for all activities pertaining to the alert memo investigations

Review
• Review of Master BMRs, BPRs. Review of protocols (sampling protocols, validation protocols, packaging protocols, study protocols, study protocols)
• Review of reports (Validation reports, Executed summary reports, packaging reports, etc.)Review of TTP documents

Candidate Profile : B.Pharm / M.Pharm / Msc with 8 to 10 years of experience

Additional Information
Experience : 8 to 10 years
Qualification : B.Pharm/M.Pharm/Msc
Location : Goa
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Quality
End Date : 30th May, 2023

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