Zenotech Laboratories Ltd (Sun Pharma) – Hiring for Computer System Validation Officer/Sr. Officer in Hyderabad

Zenotech Laboratories Limited, a subsidiary of Sun Pharma, a global leader in the pharmaceutical industry, is hiring for the role of Computer System Validation (CSV) Officer/Senior Officer at our state-of-the-art facility in Hyderabad, Telangana.

This is an exciting opportunity for professionals with expertise in computer system validation and Quality Management Systems (QMS) to join a dynamic team dedicated to ensuring regulatory compliance and quality excellence in pharmaceutical manufacturing.

Job Details

• Department: Computer System Validation (CSV)
• Position: Officer / Senior Officer
• Work Location:
  Zenotech Laboratories Limited
  Turkapally (V), Shamirpet (M), Medchal-Malkajgiri (D) – 500101, Hyderabad, Telangana State
  View Location on Google Maps

Position Requirements

• Qualification:
  • B.Tech
  • Diploma
  • B.Com
  • B.Pharmacy
• Experience: 2 to 5 years
• Notice Period: 1 to 2 months

Job Responsibilities

• Conduct computer system validation activities to qualify software systems used in pharmaceutical manufacturing.

Prepare and review critical validation documents, including:

• Validation Master Plan
• Functional Requirement Specification (FRS)
• Site Acceptance Test (SAT)
• User Manuals
• Qualification Scripts (IQ – Installation Qualification, OQ – Operational Qualification, PQ – Performance Qualification)
• Test Protocols
• Validation Summary Reports
• Periodic Review Schedules

• Ensure compliance with CSV documentation throughout different phases of the software lifecycle.
• Maintain adequate knowledge of Quality Management Systems (QMS) and apply it to validation processes.
• Perform audit trail reviews, manage data backups, and conduct periodic validations to ensure system integrity.
• Provide support during external audits and internal audits to ensure regulatory compliance.

Key Requirements

• Strong understanding of computer system validation (CSV) processes in the pharmaceutical industry.
• Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements for software validation.
• Experience in preparing and reviewing validation documentation (e.g., IQ, OQ, PQ, FRS, SAT).
• Knowledge of QMS frameworks and tools for audit trail management and data backup.
• Ability to support audits and ensure compliance with USFDA, MHRA, or other regulatory standards.
• Excellent communication skills and ability to work in a fast-paced environment.

How to Apply

• Email: Send your updated resume to hr1@zenotech.co.in.

Documents to Include:

• Updated resume
• Educational certificates (B.Tech, Diploma, B.Com, B.Pharmacy)
• Experience certificates (if applicable)
• Current CTC structure and last 3 months’ salary slips (if applicable)
• Aadhar card
• One recent passport-size photograph

Why Join Zenotech Laboratories (Sun Pharma)?

• Global Leader: Be part of Sun Pharma, one of the world’s leading pharmaceutical companies, with a strong focus on specialty generics and injectables.
• Career Growth: Develop expertise in computer system validation and regulatory compliance in a cutting-edge pharmaceutical environment.
• Supportive Environment: Work in a collaborative setting that values innovation, quality, and employee satisfaction.
• Impactful Work: Contribute to ensuring the integrity and compliance of critical software systems used in pharmaceutical manufacturing.

About Zenotech Laboratories Limited

Zenotech Laboratories Limited, based in Hyderabad, Telangana, is a pharmaceutical company specializing in generic injectables, oncology, and biotechnology products. As a part of Sun Pharma, we are committed to manufacturing high-quality pharmaceutical products that meet global regulatory standards. Our facility in Turkapally, Hyderabad, is equipped with advanced technology to support innovation and excellence in healthcare. Learn more at www.zenotechlab.com.