Quality Assurance Associate (Chennai/Indore)
Endo
Date: 3 weeks ago
City: Indore, Madhya Pradesh
Contract type: Full time
Job Description Summary
This Job role is mainly for the Documentation activity carried out at the Par formulation Indore sterile facility. The personnel will be responsible for the documentation and training management. In addition, he has to manage the different software i.e. Doc pro, Veeva and Compliance wire (LMS).
Job Description
Issuance of Record of Analysis
Isuuance of controlled copies & uncontrolled copies of the standard operating procedure
Issuance of protocols ,reports, layout and forms
Issuance of logbook and drawing
Follow the cGMP Practices as per the defined procedure
To perform Distribution ,retrevial and destruction of document as per defined procedure
To Maintain empolyee training files
To ensure document controls at site (Master production records/packaging records/Analytical documents etc )
Management of master and controlled documents in Documentation Cell
To Allot document number and equipment number as per procedure defined in procedure
Stamping of the controlled and uncontrolled copy and entry in the respective fomats.
To initiate change control related to doc cell activity
To generate Daily QMS data sheet as required and track pending task of documentation.
This Job role is mainly for the Documentation activity carried out at the Par formulation Indore sterile facility. The personnel will be responsible for the documentation and training management. In addition, he has to manage the different software i.e. Doc pro, Veeva and Compliance wire (LMS).
Job Description
Issuance of Record of Analysis
Isuuance of controlled copies & uncontrolled copies of the standard operating procedure
Issuance of protocols ,reports, layout and forms
Issuance of logbook and drawing
Follow the cGMP Practices as per the defined procedure
To perform Distribution ,retrevial and destruction of document as per defined procedure
To Maintain empolyee training files
To ensure document controls at site (Master production records/packaging records/Analytical documents etc )
Management of master and controlled documents in Documentation Cell
To Allot document number and equipment number as per procedure defined in procedure
Stamping of the controlled and uncontrolled copy and entry in the respective fomats.
To initiate change control related to doc cell activity
To generate Daily QMS data sheet as required and track pending task of documentation.
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