What You Become a Part Of

Join our Quality team to support QMS activities, quality compliance, change controls, deviations, rejection management, and quality review processes at the Pawane manufacturing site.

What To Expect
Manage Change Controls including review, evaluation, execution, post-implementation checks, and closure tracking.
Handle Deviations from review and evaluation through completion of recommended actions and closure.
Manage material rejection activities , including SAP destruction notes, approval, and tracking until physical destruction.
Prepare Inspection Plans for Semi-Finished Goods in SAP as required.
Prepare and calculate Pawane Quality Index for QMS-related parameters on a monthly basis.
Compile quality data for Monthly Quality Review Meetings, Monthly Presentations, and Quality Council Meetings .




Monitor QMS-related SOPs for effectiveness and revision in line with regulatory requirements and process changes.

Key Skills &

Competencies
Knowledge of Quality Management Systems (QMS)
Valuable understanding of Change Control & Deviation Management
Knowledge of GMP / Pharmaceutical Quality Systems
Working knowledge of SAP
Positive analytical and documentation skills
Robust follow-up and coordination skills
Good communication and presentation skills

Qualifications &

Experience
B.Pharm / M.Pharm / B.Sc. / M.Sc. or relevant qualification
Experience in Quality Assurance / QMS in the pharmaceutical industry
Experience in handling Change Control, Deviations, SOPs, Rejections and Quality Reviews preferred
Location: Pawane, Navi Mumbai
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