RayzeBio, IncHiring

Manager, Supplier Quality

  • Remote, United States
  • Lead
  • Posted 2 weeks ago
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In one line

Quality role managing GMP and GDP suppliers for a radiopharma company, covering vendor qualification, material lifecycle and audits.

About the role

On-site work with site stakeholders, other network sites and outside partners. Success means supplier activities stay compliant with global cGMPs and internal standards across clinical and commercial operations.

At a glance

Pay
Not stated in the posting
Remote scope
Remote, United States
Seniority
Lead
Skills
cGMP, GDP, CAPA, Quality Agreements, SOPs
Posted
21 Oct 2026
Last checked
3 Nov 2026

What you will do

  • Oversee qualification of GMP and GDP vendors, write quality agreements and keep the approved vendor list current
  • Run material qualification, vendor change notification and non-conformance programs, including CAPA and deviation handling
  • Take part in supplier audits as team member or lead auditor, and track observation responses to closure

What they look for

  • Experience with supplier quality in a GMP environment, including vendor qualification and quality agreements
  • Working knowledge of global cGMP and GDP requirements for starting materials, drug substance and drug products
  • Comfort leading cross-functional meetings and resolving disputes with external partners
  • Ability to review and approve SOPs, technical documents, reports and qualification records
  • Judgment to make decisions within defined practices and escalate to management when needed

Nice to have

  • Experience supporting corporate or health authority inspections

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Questions about this job

Can I do this job remotely, and from which countries?

The posting lists it as remote for people in the United States.

What does this job pay?

No pay range is stated in the posting.

What experience is needed?

It is a lead role. The posting asks for: experience with supplier quality in a GMP environment, including vendor qualification and quality agreements; working knowledge of global cGMP and GDP requirements for starting materials, drug substance and drug products; comfort leading cross-functional meetings and resolving disputes with external partners. Skills it names include cGMP, GDP, CAPA, Quality Agreements.

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RayzeBio, IncRemote, United States
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