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Associate Director Audit Inspection Jobs (NOW HIRING)

Otsuka Pharmaceutical Co., Ltd

$200 - $250/hr

R12728The Associate Director, Global Medical Review provides input into the medical review of ... This includes preparation of documentation, drafting responses to audit and inspection observations ...

Astrum Search

CT · On-site

Associate Director, SOX Internal Audit Fortune 500 Connecticut $180,000 - $190,000 + 20% bonus + stock options Astrum Search is supporting a high-growth Fortune 500 business to recruit an Associate ...

Subaru

Associate Director - Internal Audit

Camden, NJ · Hybrid

$170K - $200K/yr

SUMMARY The Associate Director of Internal Audit is the senior auditor responsible for leading the company's internal audit and warranty compliance functions along with the development ...

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How much do associate director audit inspection jobs pay per year?

As of Sep 9, 2026, the average yearly pay for associate director audit inspection in the United States is $71,776.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $81,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Associate Director Audit Inspection job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $71,776 per year, or $34.5 per hour.

Associate Director, International GVP Compliance

Boston, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$150 - $200/hr

Other

Posted yesterday

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Job description

Associate Director, International GVP Compliance (Cambridge, MA)Responsibilities / Accountabilities
  • Lead regional implementation of global GVP compliance strategies across LOCs; ensure consistent interpretation of regulations and Takeda standards.
  • Serve as regional GVP subject-matter expert; guide LOC and regional stakeholders on regulatory expectations, quality system requirements, and inspection readiness.
  • Execute/support GVP Quality System processes: deviations, investigations, CAPA management, change control, and escalation.
  • Lead high-quality investigations and root-cause analysis; ensure patient-safety focus and prevention of recurrence.
  • Track/monitor CAPA development, implementation, and effectiveness; elevate risks, delays, or systemic issues.
  • Manage inspection readiness and lead regional/LOC audits and regulatory inspections (preparation, conduct, response, follow-up).
  • Partner with Director, Regional GVP Compliance, EU QPPV and PSPV for aligned inspection messaging, issue tracking, and corrective actions.
  • Proactively identify/assess compliance risks using audit outcomes, inspection findings, KQIs, and compliance data; support governance and management review materials.
  • Support continuous improvement; develop/refine training and compliance guidance; harmonize practices across LOCs.
Qualifications (Required/Preferred)
  • Required: Scientific/allied health qualification (BSc).
  • Preferred: Advanced degree.
  • Required: 7+ years in pharma/healthcare; 4+ years in Pharmacovigilance Quality/Compliance/PV operational roles.
  • Strong knowledge of GVP regulations (EU GVP Modules, ICH E2, US CFR) and regional authority expectations.
  • Experience with GVP audits/inspections, investigations, and remediation.
  • Strong analytical/problem-solving (risk-based thinking), communication, organization, and ethical standards.
Compensation/Benefits
  • U.S. base salary range (Boston, MA): $154,400.00–$242,550.00.
  • Benefits info available via link upon application.
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