4 дня назад
Global Patient Safety Business Excellence, Senior Manager
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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