Sr. Manager IT Compliance

Job Description

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr. Manager IT Compliance Date: May 31, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Position: Senior Manager-2 Job Title: Sr. Manager IT Compliance Job Grade: G9B Function: CQ IT Sub-function: CQ IT Compliance Manager’s Job Title: DGM Skip Level Manager’s Title: NA Function Head Title: Sr. General Manager Location: Vadodara No. of Direct Reports (if any) Nil Areas of Responsibility To ensure compliance of all GxP computerized systems as per Sun CS QMS and regulatory requirements. Perform GxP computerized systems assessment referring requirement of 21 CFR part 11, EU Annex 11, applicable regulatory standards, adequate security and controls. Review of computerized systems of manufacturing systems. Emerging and Application of user privileges or access rights for entire Manufacturing and QC computerized systems. Overseeing the Manufacturing and Lab IT Compliance Viz., Setting & Verification of Security policies, Periodic Backup & Restoration activity, Investigation of backup failures, Verification windows OS policies and Active users lists for entire of Manufacturing computerized systems. Review of OEM and CSV qualification documents for manufacturing systems. Conduct Gap Assessment of GxP Computerized systems installed at Manufacturing and Lab area. Timely communicate/discuss identified gaps to responsible team. Coordinate with relevant team for compliance/closure of the identified gaps Ensure remediation of identified gaps systems compliance in timely manner with the support of team for continuous improvements Support sites to comply an internal/ external audit observation. Knowledge of Computer Software Assurance (CSA) requirements. Perform proactive assessment of regulatory and internal audit observations of one site to others Support gaps remediation programs, prioritized the remediation based on risk Provide support/guidance to remediate legacy/non-compliant computerized systems, to ensure compliance with applicable regulatory standards Support for implementing the global Quality-IT initiatives at sites Ensure key documentation of computerized systems consistently meets required quality standards throughout its lifecycle Mentor and provide support in the education and training of personnel in relevant areas of compliance and validation for GxP IT systems. Travel Estimate Frequent travel required, Approx. 70% Job Scope Internal Interactions (within the organization) With all sites (IT, QA and IT QA) External Interactions (outside the organization) Nil Geographical Scope Mumbai/Vadodara Financial Accountability (cost/revenue with exclusive authority) Job Requirements Educational Qualification B. Pharm/M.Sc. Specific Certification Nil Skills CSV, Review of GxP Manufacturing and QC systems Experience 12 Years-18 Years Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s). Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less