Ultragenyx Pharmaceutical

Associate Director, Global Inspection Management

Ultragenyx Pharmaceutical$179K — $221K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences or related field.
  • 12+ years of experience in GMP compliance or regulatory affairs in biopharmaceuticals.
  • Proven experience in leading global regulatory inspections and readiness programs.
  • Strong understanding of global GMP regulations and practices.
  • Experience with biologics or gene therapy manufacturing.
  • Excellent project management and communication skills.
  • Ability to influence across functions in a matrixed organization.

Responsibilities

  • Support the implementation of a global GMP inspection management framework.
  • Develop and maintain inspection storyboards, playbooks, and response templates.
  • Monitor and report on inspection management performance metrics.
  • Oversee coordination and response management during regulatory GMP inspections.
  • Ensure CMO sites are ready for inspections through collaboration with various teams.
  • Deliver training programs for inspection teams and SMEs.
  • Drive continuous improvement in inspection processes and tools.

Benefits

  • Generous vacation time and public holidays observed by the company.
  • Volunteer days.
  • Long-term incentive and employee stock purchase plans.
  • Employee wellbeing benefits.
  • Fitness reimbursement.
  • Tuition sponsorship.
  • Professional development plans.
Full Job Description
Position Summary:

ultracurious - Apply your biggest ideas in courageous ways

We are seeking a dynamic and experienced Associate Director of GMP Inspection Management to execute a global inspection readiness and management program. The role is accountable for the successful execution of all inspection management and readiness activities across the Ultragenyx network. This role will be responsible for ensuring consistent, proactive, and risk-based inspection readiness across internal manufacturing and testing operations, as well as external Contract Manufacturing Organizations (CMOs). The ideal candidate will bring strong expertise in GMP compliance, regulatory inspections, and cross-functional collaboration to drive a culture of continuous improvement and inspection excellence.
Work Model:

Flex: This role will typically require onsite work 2-3 days each week, or more depending on business needs. In many locations, the business will set certain days each week that Flex employees are required to be onsite.
Responsibilities:

Global Inspection Strategy & Readiness
  1. Support the implementation of a comprehensive global GMP inspection management framework and governance
  2. Support inspection readiness initiatives across internal and external manufacturing and testing sites
  3. Develop and maintain inspection storyboards/playbooks, mock inspection protocols, and response templates
  4. Monitor and report inspection management and readiness performance metrics

Inspection Execution & Management
  1. Support regulatory GMP inspections (FDA, EMA, PMDA, etc.), including coordination, and response management as needed
  2. Oversee inspection logistics, real-time support, and post-inspection follow-up activities

External Manufacturing Oversight
  1. Partner with Quality, Manufacturing, and Supply Chain teams to ensure CMO sites are inspection ready
  2. Participate in inspection readiness assessments and support CMOs during regulatory inspections

Training & Continuous Improvement
  1. Deliver inspection training programs for SMEs and inspection teams
  2. Analyze inspection trends and regulatory intelligence to inform risk mitigation strategies
  3. Drive continuous improvement in inspection readiness processes and tools.

Leadership & Collaboration
  1. Participate in cross-functional inspection readiness teams and governance forums.
  2. Collaborate with Global Quality, Regulatory Affairs, and Compliance teams to align on inspection strategy.
Requirements:
  1. Bachelor's degree in Life Sciences or related field
  2. 12+ years of experience in GMP compliance, quality assurance, or regulatory affairs within the biopharmaceutical industry
  3. Proven track record of leading global regulatory inspections and readiness programs
  4. Strong knowledge of global GMP regulations and inspection practices
  5. Experience with both internal operations and external manufacturing oversight
  6. Excellent communication and project management skills
  7. Ability to influence across levels and functions in a matrixed organization
  8. Experience with biologics or gene therapy manufacturing
  9. Prior experience working with global CMOs and managing complex supply chains
  10. Familiarity with digital tools for inspection management and quality systems
  11. Up to 25% travel may be required (Domestic and International)

#LI-KJ1 #LI-Hybrid

The typical annual salary range for this full-time position is listed below. This range reflects the characteristics of the job, such as required skills and qualifications and is based on the office location noted in this job posting. The range may also be adjusted based on applicant's geographic location.

This position is eligible for annual bonus and equity incentives. Actual individual pay is determined by demonstrated experience and internal equity alignment.

Pay Range

$179,600-$221,900 USD

Full Time employees across the globe enjoy a range of benefits, including, but not limited to:

• Generous vacation time and public holidays observed by the company

• Volunteer days

• Long term incentive and Employee stock purchase plans or equivalent offerings

• Employee wellbeing benefits

• Fitness reimbursement

• Tuition sponsoring

• Professional development plans

* Benefits vary by region and country

About Ultragenyx Pharmaceutical

Ultragenyx Pharmaceutical is a biopharmaceutical company that develops and markets treatments for rare and ultra-rare genetic diseases. The company's products are designed to address the underlying genetic causes of these diseases. Ultragenyx Pharmaceutical was founded in 2010 and is headquartered in Novato, California. The company has a number of products in development, including treatments for lysosomal storage disorders, metabolic disorders, and skeletal disorders. Ultragenyx Pharmaceutical is committed to improving the lives of patients with rare diseases and has received numerous awards for its work in this area.
Learn more about Ultragenyx Pharmaceutical
Size
1,119 employees
Market Cap
$3 billion
Industry
Net Income
-$186.5 million
Founded
2010
5 Year Trend
+383.5%
Revenue
$271 million
NASDAQ

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