Validation Analyst at Fortrea

Bengaluru, karnataka, India -

Full Time

Start Date

Immediate

Expiry Date

22 Apr, 26

Salary

0.0

Posted On

22 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation, Documentation, Project Management, Testing, Communication, Problem Solving, Attention to Detail, Analytical Skills, Teamwork, SOPs, Regulatory Compliance, Training, Mentoring, Quality Control, Process Improvement, Time Management

Industry

Biotechnology Research

Description

Job Overview: Leads validation projects as assigned and serve as a validation team member on multiple assignments as designated by the management with support from other team members as needed. Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include creating, reviewing and executing of validation documentation. Review Scope of work for the assigned project. Manage validation documentation packages including the Validation Plan, Testing Results, Traceability Matrix, and Validation Report. Assist project teams with validation tasks as requested, i.e., with the creation, production, printing and tracking of study documentation and controlled documents. Provide coordination of virtual global validation teams as needed to complete validation projects. Maintains and utilizes a strong knowledge of SOPS and validation work procedures/standards in relation to the Validation tasks. Summary of Responsibilities: Demonstrate the ability to multi-task and manage validation activities for a project effectively. Create and Execute validation test scripts and document the test results. Plan and establish timelines to meet or exceed client expectations for validations. Review clinical project specification documentation to create appropriate testing methodologies. Act as Subject Matter Expert (SME) and be point of contact for any technical services, issues related to Validation process. Write and review validation documentation to support projects. Work with other team members to create appropriate testing environments to support testing methodologies. Conduct Peer Review/Quality control of study design for assigned projects. Utilize strong working knowledge of SOPs, validation standards, and work procedures to suggest potential improvements and to provide training and guidance to all critical staff. Assist in the support of regulatory and client audits of validation activities and documents. Support management of metrics. Assist with investigating or resolving issues of patient safety or quality as directed. Understand implications of activities on project budgets. Suggest process improvements at various levels of validation process. Assist in developing key metrics for process improvement. Train, Mentor and support the team in their understanding and adoption of validation concepts and responsibilities. Active member of SOP review team as assigned. Lead or assist with special projects as designated. Perform other duties as assigned by management. All other duties as needed or assigned. Qualifications (Minimum Required): University / college degree (life sciences, health sciences, information technology or related subjects preferred). Experience and/or education plus relevant work experience, equating to a Bachelor’ s degree will be accepted in lieu of a bachelor’s degree. Fluent in English, both written and verbal). Experience (Minimum Required): 3 -5 years of relevant work experience to include Validation support and execution. Good problem-solving skills and a proactive approach. Strong communication and interpersonal skills. Good time management skills and maintain the highest standards of quality work. A neat, methodical, and thorough approach to the work with an emphasis on attention to detail. Good concentration skills are required to meet the consistently high standards expected. Self-motivation with the ability to work under pressure to meet demanding deadlines. Strong analytical skills and attention to detail. Ability to prioritize work. Effective communication skills and the ability to work as part of a team. Flexibility – being able to move from one computer system to another with ease and adapt to new technology and a constantly changing work environment. Preferred Qualifications Include: University / college degree (life sciences, health sciences, information technology or related subjects preferred). Experience and/or education plus relevant work experience, equating to a Bachelor’ s degree will be accepted in lieu of a bachelor’s degree. Fluent in English, both written and verbal). Physical Demands/Work Environment: Office work environment. Learn more about our EEO & Accommodations request here. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

Responsibilities

Lead validation projects and manage documentation requirements for Global EDC Solutions. Assist project teams with validation tasks and provide coordination for global validation teams.