Associate Director, QA – Facilities & Validation

MSD

Rahway (NJ)

Ibrido

USD 129.000 - 203.000

Tempo pieno

7 giorni fa
Candidati tra i primi
Generatore di candidature

Distinguiti per questa posizione — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Annual bonus
Long-term incentive
Medical, dental, vision insurance
401(k) retirement plan
Paid holidays

Descrizione del lavoro

Merck in Rahway, NJ is seeking an Associate Director of Quality Assurance to lead quality operations for facilities, validation, and low bioburden programs supporting clinical development at the site.

The role ensures quality systems meet regulatory standards, oversees cross-functional capital projects, and drives quality from design through startup and operations. This position expects travel and offers a comprehensive benefits package.

Competenze

  • Bachelor's degree in science, engineering, or related discipline is required.
  • Advanced degree is preferred for this role.

Mansioni

  • Lead QA activities for facilities, equipment, and automation for clinical trial material supply capabilities.
  • Support design phases and readiness of capital projects aligned with site expansion.
  • Drive quality from design through qualification, startup, and operations of new facilities; sustain existing operations.

Conoscenze

Compliance Investigations
Conflict Management
Cross-Functional Project Management
Deviation Management
Good Manufacturing Practices (GMP)
Operational Quality
Project Leadership
Project Life Cycle Management
Project Risk Assessments
Quality Assurance Systems
Quality Auditing
Quality Management
Quality Oversight
Quality Risk Management
Quality Systems Compliance
Regulatory Compliance
Strategic Thinking

Formazione

Bachelor's degree in science, engineering, or related discipline
Advanced degree preferred

Descrizione del lavoro

Merck in Rahway, NJ is seeking an Associate Director of Quality Assurance to lead quality operations for facilities, validation, and low bioburden programs supporting clinical development at the site.

The role ensures quality systems meet regulatory standards, oversees cross-functional capital projects, and drives quality from design through startup and operations. This position expects travel and offers a comprehensive benefits package.

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