Supplier Qualification Senior Specialist (6-Month Contract)
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 9d ago
The date the source published, not the day we noticed it (2026-09-23). Last seen at its source 1h ago.
We have tracked this listing since 23 Sep 2026 (8 days). The employer's own board has carried it every time we have read it, most recently 1 hour ago.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
India
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workday employer's own board first seen 8d ago · last seen 1h ago
- location not stated
The listing
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.