Fortrea has announced an opening for a Supplier Qualification Associate in Bangalore within its Supplier Qualification Office (SQO), part of Global Regulatory Compliance & Quality Assurance. This opportunity is suitable for candidates with experience in the pharmaceutical, biotechnology, CRO, clinical research, quality assurance, supplier qualification, or vendor management domains.
The Fortrea Supplier Qualification Associate job focuses on assessing and qualifying third-party suppliers whose products or services directly support clinical trials. Candidates with a bachelor’s degree, preferably in a science or business discipline, and 1–3 years of relevant life sciences industry experience are preferred.
Fortrea Job Vacancy 2026 – Overview
| Particular | Details |
|---|---|
| Company | Fortrea |
| Position | Supplier Qualification Associate |
| Department | Supplier Qualification Office (SQO) |
| Function | Global Regulatory Compliance & Quality Assurance |
| Location | Bangalore, India |
| Employment Type | Full Time |
| Qualification | Bachelor’s Degree – preferably Science or Business |
| Experience | 1–3 Years |
| Industry | CRO / Pharma / Biotechnology / Life Sciences |
| Job ID | 264933 |
| Application Deadline | September 7, 2026 |
About the Supplier Qualification Associate Role
The Supplier Qualification Associate supports Fortrea’s clinical supplier qualification process. The selected candidate will help evaluate third-party suppliers that provide products or services supporting clinical trials.
The role involves supplier quality risk assessments, qualification documentation, audit and CAPA support, Qualified Supplier List maintenance, cross-functional coordination and timely follow-up of supplier qualification activities.
Key Responsibilities
- Support qualification and capability assessment of Fortrea’s clinical suppliers under SQO management guidance.
- Coordinate supplier quality risk assessments with Quality Assurance, Strategic Sourcing and functional subject matter experts.
- Issue, collect and review supplier qualification documentation.
- Track qualification requests and ensure activities are completed within required timelines.
- Work with the broader QA team on supplier qualification audits.
- Create and maintain the Qualified Supplier List (QSL) with accurate qualification information.
- Provide support for CAPA and audit-related activities.
- Coordinate with internal and external stakeholders throughout the supplier qualification lifecycle.
- Support process improvements and other SQO initiatives as required.
Qualifications
Candidates should have a bachelor-level degree, preferably in a science or business discipline. Fortrea states that relevant and equivalent professional experience may also be considered in place of the stated educational requirements.
For life-science candidates, degrees such as B.Pharm, B.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry and related science qualifications may align with the science-degree requirement, subject to Fortrea’s screening criteria.
Candidates with business-related bachelor’s qualifications may also be considered because the official requirement specifically includes science or business disciplines.
Experience Required
Fortrea prefers candidates with 1–3 years of experience in the life sciences industry, including experience within a CRO, pharmaceutical company or biotechnology organization.
Relevant experience in areas such as Supplier Qualification, Vendor Management or Quality Assurance (QA) is particularly beneficial.
Candidates should also demonstrate:
- Strong written and verbal communication
- Project management and coordination skills
- Ability to prioritize and meet deadlines
- MS Office proficiency
- Good presentation skills
- Strong organizational abilities
- Independent and team-based working capability
- Problem-solving and process-improvement mindset
- Ability to manage multiple activities simultaneously
Why Consider This Fortrea Opportunity?
This position provides exposure to clinical supplier quality management, regulatory compliance and Quality Assurance within a global clinical research environment.
Professionals interested in building careers in clinical quality assurance, supplier quality, vendor qualification, GxP compliance, clinical audits and quality risk management may find the experience particularly relevant.
The position also involves collaboration with QA teams, Strategic Sourcing and functional SMEs, providing cross-functional exposure across clinical research operations.
How to Apply
