Trainee – Computer System Validation (CSV)

DGXPComplianceLab; Hyderabad; On-site; INR 250,000 - 350,000; Full time

Job summary

DGXPComplianceLab in Hyderabad invites you to join as a Trainee – Computer System Validation (CSV). Learn the validation lifecycle hands-on under senior CSV engineers, drafting test scripts, executing IQ/OQ steps, and recording deviations.

Ideal candidates hold a degree in pharmacy, life sciences, engineering or CS, have a basic understanding of software/databases, strong written English, and a willingness to learn GxP documentation practices; internship in pharma/QA/IT is a plus.

Qualifications

• Must have a degree in pharmacy, life sciences, engineering or computer science.
• Basic understanding of software and databases.
• Careful written English and attention to detail.
• Willingness to learn GxP documentation practices.

Responsibilities

• Draft test scripts and traceability entries under supervision
• Execute IQ/OQ test steps and capture objective evidence
• Record deviations found during testing and support their resolution
• Maintain validation document versions and review comments
• Take part in structured GAMP 5 and 21 CFR Part 11 training

Skills

Basic software/databases

Written English + attention to detail

Willingness to learn GxP documentation

Education

Degree in pharmacy, life sciences, engineering or computer science

Tools

MS Excel

Document control

Job description

Trainee – Computer System Validation (CSV)

Start a career in validating GxP computerised systems — learn the validation lifecycle hands-on under senior CSV engineers.

• Draft test scripts and traceability entries under supervision
• Execute IQ/OQ test steps and capture objective evidence
• Record deviations found during testing and support their resolution
• Maintain validation document versions and review comments
• Take part in structured GAMP 5 and 21 CFR Part 11 training

Required skills

• Degree in pharmacy, life sciences, engineering or computer science
• Basic understanding of software and databases
• Careful written English and attention to detail
• Willingness to learn GxP documentation practices

Preferred skills

• Academic project or internship in pharma, QA or IT
• Familiarity with MS Excel and document control

Project / industry exposure

• Pharmaceutical QMS, LIMS and document management systems