Thermo Fisher Scientific Hiring For Validation Analyst

Thermo Fisher Scientific is hiring for the Validation Analyst position in Bengaluru, India. The role is offered on a full-time, hybrid work basis and requires knowledge of systems validation, software validation processes, clinical trial operations, and the software development life cycle (SDLC).

Candidates with a degree in computer science, biological sciences, life sciences, or a related field, along with relevant systems or programming experience in the CRO or pharmaceutical industry, can review the eligibility criteria and apply online.

Thermo Fisher Scientific Recruitment 2026 – Job Details

Positions Available

Thermo Fisher Scientific is recruiting for the following position:

• Validation Analyst – Bengaluru, India
• Validation Analyst – Taguig City, Philippines

Responsibilities and Role Expectations

The job description outlines the following work expectations for the Validation Analyst role:

• Review and critique software development life cycle (SDLC) documentation, including requirements, functional design, system design, and test plans.
• Analyze software defects and explain how errors are produced.
• Assess the causes of test failures.
• Apply knowledge of systems and software validation processes.
• Maintain working knowledge of Good Clinical Practice (GCP), applicable standard operating procedures (SOPs/WPDs), and process maps.
• Understand clinical trial operational processes and terminology.
• Manage multiple assignments, changing priorities, and competing deadlines.
• Communicate technical information clearly and support others through teaching and guidance.

Eligibility and Qualifications

Candidates applying for the Thermo Fisher Scientific Validation Analyst job must meet the following requirements:

• A four-year degree in computer science, biological sciences, life sciences, or a related area; alternatively, an equivalent combination of education, training, and professional experience.
• Fundamental training, knowledge, and experience in systems or software validation processes.
• Two years of experience with systems or programming tools used at PPD or within the CRO/pharmaceutical industry.

Required Skills

Applicants should possess the following skills and knowledge:

• Understanding of clinical trial operations and terminology.
• Knowledge of the software development life cycle (SDLC).
• Ability to review and evaluate software development and testing documentation.
• Troubleshooting skills to analyze software defects and identify the causes of test failures.
• Working knowledge of GCP, SOPs/WPDs, and process maps.
• Proficiency in Microsoft Word, Excel, PowerPoint, and Project.
• Strong written and verbal communication skills.
• Attention to detail, analytical thinking, and problem-solving abilities.
• Client-focused approach and interpersonal skills.
• Organization, time management, and multitasking abilities.
• Ability to learn new software with minimal instruction.
• Ability to work independently and adapt to changing priorities.

Working Conditions

• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional travel to site locations may be required, including domestic and international travel.
• The role involves frequent computer use, periods of concentration, and interaction with different groups.
• Light to moderate lifting and carrying of objects, including luggage and a laptop, may be required, with a maximum weight of 15–20 lbs.