
10,000+ employees
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare • Biotechnology • Pharmaceuticals
Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.
🔥 14 hours ago
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10,000+ employees
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare • Biotechnology • Pharmaceuticals
Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.
• Support defined steps of supplier qualification and re-qualification processes • Collect, organize, and maintain supplier qualification documentation • Enter and maintain supplier data in qualification tracking systems • Support preparation of qualification packages for internal review • Assist with audit readiness by ensuring records are complete, current, and traceable • Escalate missing or inconsistent information according to SOPs • Follow procedures and processes supporting the end-to-end supplier qualification lifecycle
• Bachelor’s degree in life sciences, healthcare, quality, or related field (or equivalent experience) • 1–2 years of experience in a CRO, pharma, clinical operations, QA, or regulated industry • Exposure to document control, compliance, or operations support • Basic understanding of GCP principles • Professional, task-focused communication with internal stakeholders • Relevant and equivalent experience may be considered in lieu of educational requirements
• 6-month contract • Remote-based work • Work timings from 2 PM to 11 PM IST • EEO and accommodations support
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