Sr. Executive

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Date: Nov 5, 2025

Location: IRF - Aurangabad, MH, IN

Company: Lupin

Job Description

Supervise compliance of cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.
    Complete self-training and monitor training of team members on the relevant SOPs 
    Report any quality concern or suggestion for improvement to managers. 
    Execute and supervise all tasks and activities as per the applicable SOPs.
    Review of market complaint, OOS, OOT, deviations, incidences and participate in investigation.
    Perform quality risk assessment.
    Review of batch manufacturing record and batch packing records.
    Preparation and review of Standard Operating Procedures.
    Review, assessment and closure of change controls wherever required.
    Review, assessment and closure of other QAMS documents whenever required.
    Review of various quality system documents.
    Issuance and retrieval of SOP, various list, protocols and logbooks etc.
    Review of Annual Product quality review reports.
    Handling of recall and returned goods.
    Maintain all cGMP records.

Work Experience

8-12 years

Education

Graduation in Pharm D Degree

Competencies

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