Job
Description
Roles and Responsibilities:
- Act as administrator in Operating Systems (OS) and Instrument/Equipment connected application software (including CDS - Empower, Chromeleon, DCS, DAS etc.) in QC/Production areas for Systems Administration, Troubleshooting, and Data Backup/Restore Management.
- Responsible for identifying the data from instrument/equipment connected application software in QC/Production areas; schedule their backups in backup solution software (i.e. veritas Backup exec) and maintain the list as per SOP requirements.
- Responsible for Performing/Monitoring the data backup as per schedule or manually and maintain the backup media and activities logs as per SOP requirements.
- Responsible for Performing the data restore on user's requests/periodically, verify it along with users and maintain their activities logs in line to SOP requirements.
- Responsible for performing and maintaining the activities logs logging the applications administration activities such as System Configuration & Security Policies Implementation, Privileges & Roles Management, User Management - User Creation, Modification, Enable/Disable, Lock/Unlock etc.) as per SOP for the Quality Control Labs & Manufacturing systems.
- Responsible for implementing the required security patches at OS level on instruments/equipment's connected GxP computer systems in QC & manufacturing areas.
- Responsible for verification and correction of date & time on QC instruments and standalone GxP computer systems.
- Responsible for performing the changes in instruments/equipment connected applications software in QC/Production areas as per change management procedure.
- Responsible for completing/implementing the sites IT related Change Controls, Deviations, Investigation Reports, CAPAs, and Audit Observations if any.
- Responsible for execution of computer systems qualification and validation (CSV) activities in QC/Production areas systems as per Computer Systems Validation requirements.
- Responsible for facing the internal/regulatory audits and will able to demonstrate the required compliance & controls are in place w.r.t. IT systems administrations, Operations, data backup/restore, security, tractability and integrity to the auditors on demand.
- Responsible for implementing the required new/revised SOPs at sites and ensuring the overall compliance of the same.
- Responsible for maintaining the updated list of instruments/equipment connected applications software in QC/Production areas as per change management procedure
Interview Venue- Gland Pharma Unit 2, Plot No: 42-52., Phase III, TSIIC. Pashamylaram. Patancheru, Hyderabad, Medak, Telangana, India
Interview Date & Time – 10th & 11th Dec b/w 9:00 AM-12:30 PM
Work location- Pashamylaram ( Sangareddy )
Remote Working- No (Work from Office)
Mandatory Documents: 10th,12th , UG, PG marks memo, Last three months’ Salary slips, Latest Increment Letter/CTC letter, Last three months Bank Statement
Please Note: Candidates who have been interviewed in the last 6 months are not eligible.
Sangareddy, Pashamylaram