Associate Validation Analyst Job at Thermo Fisher Scientific
Job Type: Full-Time
Work Mode: Hybrid
Shift: Second Shift (1:00 PM – 10:00 PM IST)
Experience Required: 1–2 Years
Job Location:
- Bengaluru, India
- Taguig City, Philippines
Application Type: Online Application
Job Status: Verified Job
Job Overview
Thermo Fisher Scientific, a global leader in life sciences and healthcare solutions, is hiring an Associate Validation Analyst (CSV) to support validated software systems in regulated environments. Associate Validation Analyst Job
This hybrid role is ideal for professionals with 1–2 years of Computer System Validation (CSV) or validation experience within pharma, CRO, or regulated clinical settings. The position focuses on Performance Qualification (PQ), change control, and validation lifecycle activities, supporting global stakeholders in a structured compliance-driven environment.
Candidates willing to work in a second-shift schedule and looking to build a long-term career in pharma validation, compliance, and regulated systems are encouraged to apply. Associate Validation Analyst Job
Key Responsibilities – Associate Validation Analyst
- Provide business and system support for validated software and computerized systems
- Participate in CSV and Performance Qualification (PQ) activities across the Software Development Life Cycle (SDLC)
- Prepare, review, and maintain Validation Plans, PQ Test Cases, and Validation Summary Reports
- Author, execute, and document PQ test scripts with complete and accurate compliance evidence
- Review and support Change Control documentation in accordance with established SOPs
- Assist in system upgrades, enhancements, and validation testing activities
- Support users during system implementation and post-deployment phases
- Participate in Periodic Reviews to ensure the Master Validation Plan remains current
- Ensure data integrity, testing accuracy, and adherence to regulatory requirements
- Collaborate with cross-functional and global stakeholders to support validation objectives
Associate Validation Analyst Job
Eligibility and Qualifications
Education
- Bachelor’s degree or equivalent qualification
- Preferred fields include Science, Pharmacy, IT, Engineering, or related disciplines
Experience
- Minimum 1 year of Computer System Validation (CSV) experience – Mandatory
- 1–2 years of experience in validation, testing, or regulated environments
- Experience in pharma, CRO, or life sciences industries is preferred
Associate Validation Analyst Job
Required Skills
- Strong written and verbal communication skills
- Hands-on experience with PQ documentation and test execution
- Working knowledge of pharma regulatory and compliance requirements
- High attention to detail with strong analytical and problem-solving abilities
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Customer-focused mindset with adaptability to changing priorities
- Ability to work collaboratively in cross-functional teams
Associate Validation Analyst Job
Work Schedule and Location
Work Mode: Hybrid
Shift Timing: 1:00 PM – 10:00 PM IST
Job Locations:
- Bengaluru, India
- Taguig City, Philippines
Candidates must be comfortable working in an afternoon/evening shift aligned with global operations.
Salary and Benefits
Estimated Salary (India): ₹4,00,000 – ₹7,00,000 per annum
Benefits Include:
- Hybrid working model
- Exposure to global validation and regulated systems
- Structured learning in CSV and validation lifecycle
- Career growth opportunities in pharma compliance and quality systems
- Stable work environment within a globally recognized organization
Note: Salary may vary based on experience, skills, and interview performance.
Why Join Thermo Fisher Scientific
- Work with a globally trusted name in life sciences and healthcare
- Gain hands-on experience in regulated and validated environments
- Build a strong foundation in Computer System Validation (CSV)
- Collaborate with international teams and stakeholders
- Access long-term career growth in compliance, quality, and validation domains
Associate Validation Analyst Job
How to Apply
Interested candidates can apply online through the official application link provided by the employer. Ensure your resume highlights CSV experience, PQ documentation, validation activities, and regulated environment exposure.
Early applications are encouraged, as verified roles may close once positions are filled. Associate Validation Analyst Job
For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.
Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
