Jobs
Third Party Management Specialist
| Posted On: Mar 19, 2026
Framingham, MA 01701
6 Months, Contract
On-site
Job Summary
- Job Title:
- Third Party Management Specialist
- Posted Date:
- Mar 19, 2026
- Duration:
- 6 Months, Contract
- Shift(s):
-
09:00 - 17:00
- Salary ($):
- 61.58 - 63.75 per Hourly (compensation based on experience and qualifications)
- We care about you! Explore Rangam’s benefits information
Talk to our Recruiter
- Name:
- Mittul Yadav
- Email:
- mittul@rangam.com
- Phone:
- 984-422-4083
Description
Free parking Prefer local candidates only Contract only approved for 6 months
Title: Third Party Management Specialist Some slight flex on schedule start/ stop time Fully onsite position/ Free parking onsite *Local candidates only
- Role will work with some of the smaller vendors, will reach out to and worker,
- This is not a post market compliance role, this is on material compliance role – single use system, defects of materials, they’ll reach out to supplier to conduct investigations.
Must have:
- Must have bachelor’s degree + 6 years of applicable experience
- Manager is open to all levels of experience
- Experience communicating with 3rd parties, understanding of 3rd party relations with impact QMS, quality agreements.
- Vendor pass, quality agreements, supplier change notification
Nice to have:
- Previous experience with Veeva, quality agreements, supplier compliance, supplier change notifications preferred, SAP
Description:
- The Third Party Management Specialist will oversee Third Party Quality operations for the MA Bio Campus, ensuring excellence in quality standards and regulatory compliance across external partnerships.
- This role requires leading Supplier Change Notification (SCN) processes, managing third party quality event investigations, supporting quality agreement programs including periodic reviews and documentation, and collaborating cross-functionally with QC, Facilities, and Manufacturing departments to resolve compliance issues.
- The ideal candidate will have a Bachelor's degree or equivalent experience in Supplier Quality, minimum 6 years of Quality/Operations experience in a biotech/pharmaceutical cGMP manufacturing environment within an FDA-regulated industry, proficiency in Veeva quality management systems, and strong knowledge of global pharmaceutical regulations (US, EU, Canada, Japan, Australia).
- This position reports to the Head of Quality Third Party and requires the ability to gown and enter manufacturing