SU

Manager - Corporate Quality Audit

Sun Pharma
Bangalore10-15 LPA Posted 28 Apr 2025
FULL TIME
Manufacturing Process
Quality Systems
MHRA
Quality Assurance
Quality Audit

Job Description

Position: Manager (G10) Effective Date:

Department: Corporate Quality Location: Bengaluru,

Reporting Manager Title: GM - Corporate Quality

Classification: Manager - Corporate Quality (Gamma Irradiation)

Job Summary:

  • Manager Corporate Quality - Individual Performer Role
  • Responsible for oversight of Gamma Irradiation of Sun Pharma products at third party gamma irradiation sterilization.

Essential Job Functions:

  • Should possess sound knowledge of pharmaceutical manufacturing process (Non-sterile & Sterile formulations) & quality assurance regulations and auditing technique.
  • Responsible for the overall supervision of Gamma sterilization site (Third party) used for sterilization of drug product and other components, as required.
  • To monitor receipt and dispatch of consignment of Sun Pharma at Gamma sterilization site.
  • Review and monitoring of irradiation process of the batch and related documentation.
  • Review and monitor of analytical data (Dosimeter Testing)
  • Control and monitor quality systems which enable operations on site to occur in an efficient manner and in compliance with cGMPs.
  • Follow-up for timely closure of QMS documents.
  • Participating in the investigations for Deviations, OOS and Audit findings related to Sun Pharma product/s.
  • Review of changes in gamma sterilization process / major modification at site and timely notification to the management.
  • Supporting in external audits preparations and responding to audit findings of gamma serialization sites
  • Should be able to travel to third party site/s.
  • Basic computer skills (Microsoft word/ Excel/ Power point presentation) and ability to learn and become proficient with appropriate software.
  • Should possess good verbal and written communication skills.

Basic Qualification: B. Pharm / MSc

Industrial Experience & Knowledge:

  • Minimum work experience of 10-15 Years in formulation & quality systems management operations.
  • Exposure to regulatory agencies audits such as Schedule - M, USFDA, MHRA, ANVISA, TGA, WHO, ISO etc.
  • Knowledge of Track wise/LIMS/SAP is desirable.
  • Ability to work effectively in multicultural matrix organization.

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