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4 дня назад

Global Patient Safety Business Excellence, Senior Manager

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Global Patient Safety Business Excellence, Senior Manager (Pharmacovigilance/Business Excellence): Driving project management, governance, compliance, and operational effectiveness initiatives across Global Patient Safety with an accent on inspection readiness, quality systems, and organizational change. Focus on leading complex cross-functional programs, managing pharmacovigilance activities for mergers and divestitures, and applying automation, analytics, and emerging technologies to improve business outcomes.

Location: Washington D.C., District of Columbia, United States

Company

hirify.global is a biotechnology company that researches, manufactures, and delivers medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Lead project management, change management, governance, and business excellence initiatives across Global Patient Safety.
  • Deliver business-critical and enterprise-wide cross-functional programs.
  • Provide oversight for pharmacovigilance activities related to mergers, acquisitions, licensing agreements, and divestitures.
  • Advance the Global Patient Safety Quality Management System and maintain inspection readiness.
  • Support health authority inspections, business partner audits, internal process audits, deviations, CAPAs, and quality improvement initiatives.
  • Develop compliance and performance metrics and champion automation, analytics, and emerging technologies.

Requirements

  • Doctorate degree and 2 years of safety project management experience; or master's degree and 4 years; bachelor's degree and 6 years; associate's degree and 10 years; or high school diploma/GED and 12 years.
  • Significant experience in pharmacovigilance, drug safety, regulatory affairs, quality, or related life sciences functions.
  • Expertise in project management, change management, organizational transformation, governance frameworks, and complex enterprise-wide initiatives.
  • Experience working with pharmacovigilance regulations, compliance practices, inspections, audits, and quality systems.
  • Strong analytical, leadership, facilitation, decision-making, and stakeholder-influence skills.
  • Experience with process improvement methodologies such as Lean, Six Sigma, Agile, or equivalent; PMP or change/project management certification is preferred.

Nice to have

  • Experience with mergers, acquisitions, and divestitures in life sciences.
  • Experience leading fully remote teams across time zones.
  • Experience presenting to and influencing senior leadership and executive stakeholders.

Culture & Benefits

  • Collaborative, innovative, science-based working environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus, stock-based long-term incentives, and award-winning time-off plans.
  • Flexible work models where applicable, plus career development opportunities.

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