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Validation Analyst
full-timeBengaluru

Summary

Location

Bengaluru

Type

full-time

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About this role

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.

Other facts

Tech stack
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

About Fortrea

Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Biotechnology Research

What you'll do

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

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Frequently Asked Questions

What does a Validation Analyst do at Fortrea?

As a Validation Analyst at Fortrea, you will: lead validation projects and manage documentation requirements for Global EDC Solutions. Assist project teams with validation tasks and provide coordination for global validation teams..

Why join Fortrea as a Validation Analyst?

Fortrea is a leading Biotechnology Research company.

Is the Validation Analyst position at Fortrea remote?

The Validation Analyst position at Fortrea is based in Bengaluru, India. Contact the company through Clera for specific work arrangement details.

How do I apply for the Validation Analyst position at Fortrea?

You can apply for the Validation Analyst position at Fortrea directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Fortrea on their website.