Jobs

Third Party Management Specialist

|  Posted On: Mar 19, 2026

location:Framingham, MA 01701

Duration:6 Months, Contract

mode of work:On-site

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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)
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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