Senior Manager, Global Clinical Supplier Quality

Insmed

New York (NY)

Vor Ort

USD 180.000 - 230.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Insmed seeks a Senior Manager of Clinical Supplier Quality to lead supplier oversight and compliance across global clinical development programs. You will manage qualification, performance monitoring, quality agreements, and regulatory inspections to ensure adherence to GCP standards and quality expectations.

In this role, you will drive supplier qualification, risk assessment, and lifecycle governance while partnering with cross-functional teams to uphold data integrity and regulatory readiness

Qualifikationen

  • Bachelor's degree required in a relevant field and 12+ years GCP-regulated experience.
  • Experience leading supplier quality programs for outsourced clinical and nonclinical providers.
  • Strong knowledge of ICH GCP guidelines, data integrity, and risk-based quality management.

Aufgaben

  • Lead supplier qualification, onboarding, risk assessment, and lifecycle management for clinical suppliers and service providers
  • Maintain approved supplier list and qualification records with risk-based controls throughout supplier lifecycle
  • Administer supplier escalation programs and performance monitoring frameworks including KPIs, scorecards, and quality metrics
  • Manage supplier quality events, deviations, investigations, CAPAs, and develop quality procedures and governance frameworks
  • Develop and manage global Quality Technical Agreements; support audit programs and health authority inspection readiness activities

Kenntnisse

GCP supplier oversight
CAPA management
Quality risk management
Data integrity principles
Audits
Regulatory inspections readiness
Negotiation
Analytical skills
Organizational skills

Ausbildung

Bachelor's degree in Chemistry, Engineering, Life Science, or related field

Jobbeschreibung

Insmed seeks a Senior Manager of Clinical Supplier Quality to lead supplier oversight and compliance across global clinical development programs. You will manage qualification, performance monitoring, quality agreements, and regulatory inspections to ensure adherence to GCP standards and quality expectations.

In this role, you will drive supplier qualification, risk assessment, and lifecycle governance while partnering with cross-functional teams to uphold data integrity and regulatory readiness

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