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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Director Device Operational QA

Regulatory & Quality (Life Sciences)Posted on Nov 10
Full-timeBoston, MA, USA

About the Job

Requirements

  • Strong knowledge of Device Operational Quality Assurance and quality-system principles.
  • Knowledge of applicable regulatory and ISO-related requirements for operational quality oversight.
  • Knowledge of quality risk management and risk-based decision-making.
  • Knowledge of quality-event management, including deviations, nonconformances, investigations, corrective and preventive actions, and change control.
  • Knowledge of quality documentation, record review, and approval practices.
  • Knowledge of audit and inspection readiness activities.
  • Ability to lead, develop, and motivate teams within a quality organization.
  • Ability to assess complex quality matters, identify risks and trends, and appropriately escalate issues.
  • Strong cross-functional collaboration, stakeholder management, and influencing skills.
  • Ability to prioritize competing demands and drive execution in a complex operational environment.
  • Strong written, verbal, presentation, and interpersonal communication skills.
  • Demonstrated commitment to quality, compliance, continuous improvement, accountability, and sound judgment.
  • Typically requires 12 or more years of relevant work experience and 5 years of supervisory or management experience, or an equivalent combination of education and experience.
  • Significant progressive experience in quality assurance, quality systems, operational quality, manufacturing quality, or a related regulated environment.
  • Demonstrated experience supporting design control and risk management activities for medical devices and combination products.
  • Demonstrated people-management experience, including coaching, performance management, talent development, and team leadership.
  • A minimum bachelor's degree in a scientific, engineering, allied health, or related field.

Responsibilities

  • Lead, coach, and develop the Device Operational Quality Assurance team; establish clear priorities, performance expectations, and development plans.
  • Provide quality oversight for device operational activities and ensure consistent execution of applicable quality-system processes and standards.
  • Serve as a key quality partner to cross-functional teams supporting device programs and operations.
  • Lead assessment, resolution, communication, and escalation of complex operational quality issues and risks.
  • Ensure appropriate oversight of quality events, including deviations, nonconformances, investigations, corrective and preventive actions, and change controls, as applicable.
  • Provide direction for the review and approval of device-related quality documentation and records, including design controls and risk management at a minimum.
  • Monitor operational quality performance, metrics, trends, and emerging risks; communicate findings and recommendations to Quality leadership and key stakeholders.
  • Support and maintain audit and inspection readiness for device operational activities.
  • Drive continual improvement of Device Operational Quality Assurance processes, procedures, tools, and ways of working.
  • Promote risk-based decision-making, accountability, collaboration, and a culture of quality across device operations.
  • Contribute to functional planning, quality strategy, and capability-building initiatives in partnership with senior Quality leadership.
  • Ensure timely execution of quality commitments and appropriate follow-up on actions, decisions, and escalated matters.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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