Job Overview:
Provide foundational operational support to the supplier qualification lifecycle, ensuring accurate documentation and compliance with procedures.
Summary of Responsibilities:
- Support defined steps of the supplier qualification and re‑qualification processes.
- Accurately collects, organizes, and maintains 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 life cycle.
Qualifications (Minimum Required):
- Bachelor’s degree in life sciences, healthcare, quality, or related field (or equivalent experience)
Experience (Minimum Required):
- 1-2 years of experience in a CRO, pharma, clinical operations, QA, or regulated industry
- Exposure to document control, compliance, or operations support
- Understands basic GCP principles
- Professional, task‑focused communication with internal stakeholders
Preferred Qualifications Include:
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Physical Demands/Work Environment:
- Remote-Based, as requested by the line manager
- Work Timings: 2 PM to 11 PM IST.
Learn more about our EEO & Accommodations request here.
Skills Required
- Bachelor's degree in life sciences, healthcare, quality, or a 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 Good Clinical Practice principles
- Professional, task-focused communication with internal stakeholders
- Relevant equivalent experience may substitute for educational requirements
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
