Job Description

Qualification : B Pharm/ M. Pharm

Experience : 15 to 20 years.

Job Responsibilities

  • Ensure compliance of all procedures, practices and system to cGMP with respect to Schedule M., WHO guidelines, Abbott Quality guideline and Standard operating procedures at site.
  • Responsible for QMS.
  • To review and approve the investigation reports of Exception and market complaint.
  • To review and approve the change control, planned deviation in track wise.
  • To review and approve the site complaint investigation and accountable for timely closure of site complaints.
  • To review the CAPA and track its implementation within the timeframe. To check the effectiveness of CAPA implemented.
  • To monitor the site internal audit program and its compliance. Participation as an Auditor in internal audit.
  • To ensure implementation of EQD Policies on site within the given timeframe.
  • Management of D...

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