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

Sun Pharma Laboratories Ltd; Gangtok; On-site; INR 1,00,000 - 4,50,000; Full time

Job summary

An established industry player is seeking a dedicated Team Member for Plant IT to enhance their Quality Informatics systems. In this pivotal role, you will be responsible for managing and supporting software related to laboratory instruments as an Application Administrator. This includes user management, backups, and ensuring compliance with quality standards. You will play a crucial role in maintaining data integrity and supporting regulatory audits. If you have a passion for IT and quality compliance in a dynamic environment, this opportunity is perfect for you to make a significant impact in the field of pharmaceuticals.

Qualifications

• 4-6 years of experience in IT administration, particularly in laboratory environments.
• Strong knowledge of software management for laboratory instruments.

Responsibilities

• Support Quality Informatics and manage software for laboratory instruments.
• Conduct user management and ensure compliance with IT regulations.

Skills

User Management

Backup and Restoration

Validation and Qualification

Software Administration

Quality Control Compliance

Education

BE/B. Tech

MCA

BCA

MSc IT

BSc IT

Graduation + PGDCA

Tools

Laboratory Instruments Software

Windows Operating System

Job description

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 related to Laboratory Instruments/Equipment as an Application Administrator. Responsibilities include user management, backups, archival, restorations, periodic reviews, validation, and qualification.

Key Responsibilities:

1. Maintain software related data of Laboratory Instruments/Equipment as an Application & System Administrator.
2. Create, modify, disable, and re-activate User Account(s) and assign privileges for both Windows & application.
3. Prepare and review configuration specification documents.
4. Prepare and review standard operating procedures associated with the planning, development, and operation of IT related systems.
5. Perform activities related to server software such as project creation, template migrations, archival/backup of soft data, and restore projects.
6. Manage standalone Laboratory instrument software including archival/backup and restoration.
7. Prepare periodic review schedules and execute reviews of each instrument accordingly.
8. Control and maintain passwords for Analytical Balances, pH meters, and Stability chambers (HMI) used in the Quality Control Laboratory.
9. Prepare validation/review documents such as requirement specifications, validation plans, test plans, summary test results, and final validation reports.
10. Conduct IT activities related to IQ/OQ/PQ and configuration policies for Laboratory instrument/Equipment software.
11. Coordinate and verify that all validation activities and documents comply with applicable regulations and internal procedures at all locations.
12. Contribute to QMS activities such as CCRs, incidents, deviations, and CAPAs related to IT systems in a timely manner and maintain IT regulations & compliance.
13. Support the design/implementation and ensure compliance with all quality-related policies, standards, and IT systems at QC of the site.
14. Facilitate internal and regulatory agency audits, ensuring findings from site QC audits are understood, assessed, and addressed comprehensively.