Pharma IT (Quality Management System) Profile
Job Description:
• Ensure cGMP, Good Documentation Practices (GDP), Data Integrity, and Data Security Policies are followed.
• Oversee and validate various software in quality control and assurance functions, such as HPLC, IR, UV, and Stability Control systems.
• Manage user accounts, roles, and access rights for quality systems and instruments.
• Backup/archive QC data and ensure its secure storage and restoration.
• Perform administrative tasks for software and hardware systems used in QA/QC departments.
• Coordinate remediation of IT controls in manufacturing systems, focusing on deletion restrictions, user access management, and data backup.
• Conduct cross-functional activities with other departments to ensure alignment with quality standards.
• Train quality control staff on IT system usage and data security practices.
• Monitor and review QMS activities to identify areas for process improvement.
• Lead audits to ensure compliance with regulatory requirements in IT and QMS domains.
• Stay updated with evolving regulatory guidelines in the pharmaceutical sector.
Company Profile
Our client followa standards of WHO - CGMP
Our Mission
“To become a valued Pharmaceutical partner to the World Pharma fraternity by continuously researching, developing and manufacturing a wide range of pharmaceutical products that complies with the global regulatory standards.”
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.