ElancoHiring

Executive Director, Quality, Global Biologics Network

  • Remote, United States
  • Lead
  • Posted 5 days ago
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In one line

Top quality role overseeing biologics manufacturing sites worldwide, setting the quality strategy and answering to regulators.

About the role

Accountable for quality across every internal biologics plant, including inspection readiness and risk management. The person sits with manufacturing, technical services and supply chain leaders to keep product flowing.

At a glance

Pay
Not stated in the posting
Remote scope
Remote, United States
Seniority
Lead
Skills
cGMP, Quality Risk Management, LEAN, Biologics manufacturing, Vaccines manufacturing, Health authority inspections
Posted
30 Oct 2026
Last checked
2 Nov 2026

What you will do

  • Set the global quality strategy, risk framework and lifecycle management for biologics sites
  • Run health authority inspection readiness and roll out standards across internal and partner sites
  • Track quality KPIs and apply risk management methods to drive continuous improvement
  • Build quality talent and is the final escalation point for critical quality issues

What they look for

  • Bachelor's degree in a science or engineering field such as chemistry, microbiology or pharmacy
  • At least 15 years in pharmaceutical or biotech quality assurance or operations, with 10 or more in senior leadership
  • Deep knowledge of biologics and vaccine manufacturing and of FDA, EMA and USDA cGMP rules
  • A record of leading international health authority inspections and developing quality teams

Nice to have

  • A master's or PhD in life sciences, management or a related science field

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Questions about this job

Is this job fully remote, and from where?

Yes, it is listed as remote, aimed at 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 lead role. The posting asks for: bachelor's degree in a science or engineering field such as chemistry, microbiology or pharmacy; at least 15 years in pharmaceutical or biotech quality assurance or operations, with 10 or more in senior leadership; deep knowledge of biologics and vaccine manufacturing and of FDA, EMA and USDA cGMP rules. Skills it names include cGMP, Quality Risk Management, LEAN, Biologics manufacturing.

How do I apply with Keywordise AI?

Press the Apply with Keywordise AI button and add your CV. Keywordise tailors your CV and cover letter to this posting and sends the application for you, with a free 7-day trial and no card.

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