Job Description
**Qualification : B Pharm/ M. Pharm**
**Experience : 15 to 20 years.**
**J** **ob 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 ...
**Experience : 15 to 20 years.**
**J** **ob 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 ...
Apply for this Position
Ready to join Abbott? Click the button below to submit your application.
Submit Application