Manager Production Liquid Orals External Preparations

Agio Pharmaceuticals Limited

Pune District

On-site

INR 600,000 - 900,000

Full time

5 days ago
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Job summary

Agio Pharmaceuticals Limited in Pune is seeking a Production/Manufacturing Executive to oversee liquid oral and topical dosage form manufacturing, filling and packing with strict adherence to cGMP. You will prepare and execute weekly and monthly production plans, ensure batches conform to product registrations, and review SOPs.

The role involves QMS activities, CAPA, change control, audits, and cross-functional coordination.

Qualifications

  • Manufacturing, filling & packing of Liquid Orals.
  • Manufacturing, filling & packing of Ointment, Gel, cream.
  • Preparation and execution of Weekly & Monthly Production Plan.
  • Adherence to cGMP guidelines.

Responsibilities

  • Verify breakdown and maintenance of facilities and equipment.
  • Review and approve BMR/BPR/Protocol; cross-functional QMS.
  • Manage QMS activities like change control, deviation, CAPA.
  • Prepare for audits and ensure compliance with production standards.
  • Work allocation and online document verification.

Job description


  • Responsible for manufacturing, filling & packing of Liquid Orals.
  • Responsible for manufacturing, filling & packing of Ointment, Gel, cream.
  • Responsible for preparation and execution of Weekly & Monthly Production Plan.
  • Responsible for accomplishment of the target with strict adherence and compliance to the guidelines of cGMP.
  • Responsible to ensure that the batches manufactured in accordance with the product registration
  • Preparation and Review & Implementation of Standard Operating Procedures of production department
  • Handling of QMS activities like change control, deviation, CAPA
  • Responsible for review and approval of BMR / BPR / Protocol / and cross functional QMS
  • Responsible for Audit preparations and Compliance.
  • Responsible for accomplishment of the target with strict adherence and compliance to the guidelines of cGMP.
  • Responsible for work allocation and online documents verification.

Responsible to verify the breakdown, maintenance of facilities and equipments.


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