Posted:2 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Should have worked in Managerial capacity in Pharmaceutical API Intermediate/CDMO manufacturing set ups

Responsible for Daily Production activities as per the monthly plan

Responsible for Yield and Quality improvement and it’s monitoring

Responsible for RMC and productivity

Responsible for Raw Material Planning in coordination with Stores Department

Responsible for monitoring and reduction of production cycle time

Prepare Monthly reconciliation Report

Effective handling of available resources and manpower

Ensure all the processes are carried out as per cGMP guidelines in coordination with Quality Assurance Department

Review the filled BPR after completion of batch

Review the BPR, SOP, validation protocol, and other production related documents

Initiation of change control for any change in production related activities

Evaluate, investigate, and report critical deviations, OOS, complaints, and material returns etc.

Responsible for training to Production employees and timely review the performance standards


Education : BE chemical

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