Sun Pharma Laboratories Ltd Looking for Team Member – Plant IT at Ranipool, Sikkim Full Time

Title: Team Member – Plant IT

Date: Oct 3, 2022

Location: Sikkim II – Plant

Company: Sun Pharma Laboratories Ltd

Position: Officer IT

Grade: G12C

No of Positions: 1

Experience: 4 – 6 Years

Job Location: Sikkim-II

Education: BE/B. Tech, MCA, BCA, MSc IT, BSc. IT, Graduation + PGDCA.

Job Profile:
The Job holder will be responsible to support Quality Informatics and manage the software’s related of Laboratory Instrument / Equipment’s as an Application Administrator and perform the activities of Laboratory instruments such as User Management, Backups, Archival, Restorations, Periodic Reviews, validation & qualification etc.

To maintain software related data of Laboratory Instrument / Equipment’s as an Application & System. Administrator.

To perform activities like creation / modification /Disable / Re-activation of User Account(s) and assigning of privileges for both windows & application.

To prepare, review configuration specification documents.

To prepare and review standard operating procedures associated with the planning, development and operation of IT related systems.

To perform the activities of Server software like: Project creation, template migrations, Archival / backup of soft data, Restore projects.

To perform the activities of standalone Laboratory instruments software’s like Archival / backup, restoration etc.

To prepare periodic review scheduler and execute periodic review of each instrument accordingly.

To control and maintain the Password of Analytical Balances, pH meter and Stability chambers (HMI) used in the Quality Control Laboratory.

To prepare validation / Review documents such user as requirement specifications, validation plans, test plans, summary test result and final validation reports.

IT activity related to IQ/OQ/PQ and configuration policies for Laboratory instrument / Equipment’s software.

To coordinate and verify that all validation activities and documents comply with applicable regulations and internal procedures at all locations.

To contribute in QMS activities such as CCRs, incidents, deviations and CAPAs related to IT systems in a timely manner and Maintain IT regulations & compliance all the time and regulatory audit support at sites.

To support for designing/implementing and ensuring compliance to all quality related, Policies, Standards and IT systems at QC of the site.

Facilitate internal and regulatory agency audits, ensuring that findings from site QC audits are understood, assessed and addressed site wise in a comprehensive manner.