RayzeBio, IncHiring

Senior Supplier Quality Auditor

  • Remote, United States
  • Senior
  • Posted yesterday
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In one line

Audit role for a quality professional with at least seven years in pharma or biotech, leading supplier audits and tracking fixes to closure.

About the role

Suits someone who can work alone, judge quality risks and write clear audit reports, while dealing with suppliers and internal teams.

At a glance

Pay
Not stated in the posting
Remote scope
Remote, United States
Seniority
Senior
Skills
cGMP, GxP, EudraLex Volume 4, ICH Guidelines
Posted
28 Oct 2026
Last checked
28 Oct 2026

What you will do

  • Plan and run supplier audits on site and remotely, following the approved audit programme
  • Check suppliers against FDA, EMA and ICH rules, internal procedures and quality agreements
  • Write up audit findings and agree corrective actions with suppliers and internal teams
  • Follow corrective actions until they are finished, and keep audit records complete
  • Help prepare for regulatory inspections linked to supplier oversight
  • Train suppliers and internal teams on audit processes and GxP expectations

What they look for

  • At least seven years in quality assurance, auditing or supplier management in pharma, biotech or a cGMP setting
  • At least three of those years spent auditing or doing quality assurance in a regulated environment
  • Working knowledge of 21 CFR Parts 11, 210 and 211, EudraLex Volume 4 and ICH guidelines
  • Audit experience across GMP, GLP or GCP
  • Ability to spot systemic quality and compliance risks and write strong technical reports

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Questions about this job

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

Yes. The posting lists Senior Supplier Quality Auditor as a remote role for candidates in the United States.

What does this job pay?

No pay range is stated in the posting.

What experience is needed?

It is a senior role. The posting asks for: at least seven years in quality assurance, auditing or supplier management in pharma, biotech or a cGMP setting; at least three of those years spent auditing or doing quality assurance in a regulated environment; working knowledge of 21 CFR Parts 11, 210 and 211, EudraLex Volume 4 and ICH guidelines. Skills it names include cGMP, GxP, EudraLex Volume 4, ICH Guidelines.

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