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Job Overview

  • Date Posted
  • Location (State / UT)
  • Expiration date
  • Experience
    25 Years +
  • Gender
  • Desired Qualification
    Master’s Degree, Doctorate Degree
  • Salary in (₹)

Job Description

Key responsibilities:

  • Responsible for planning and execution of the overall quality compliance strategy and ensuring the highest level of compliance across all the plants by institutionalizing the compliance framework.
  • Responsible for annual audit plans, developing training plans based on needs and assessments, and ensuring alignment with the overall quality agenda across all the sites.
  • Responsible for the implementation of a Quality management system across all sites.
  • Establishments of robust QMS for delivering mission-critical results with a focus on the delivery of superior quality benchmarks.
  • The activities included continuous improvement initiatives through risk management, continuous regulatory surveillance, and CAPA analysis to ensure regulatory requirements.
  • Should Involve directly in regulatory Audits at sites like USFDA, MHRA, WHO, and ANVISA, Self-Inspections, Vendor audits, Corporate Quality audits gap assessments, etc, and timely submission of responses to Health Authorities and response to regulatory queries.
  • Should Monitor teams on deliverables, track and periodically present KQIs, KPIs, and GMP training, exchange best practices of the site, keeping management informed of quality status.

Qualification: Ph.D./M.Pharm/ M.Sc.

Location: HO, Vakola

Experience: 25 28 Years

Age: 45-50 Years