5 дней назад
Manager, Project Management – Technical Operations (Biopharma)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Manager, Project Management – Technical Operations (Biopharma): Leading cross-functional pharmaceutical and biotech programs from research through development, regulatory submission, launch, and lifecycle management with an accent on project governance, risk mitigation, technical operations, and external partner coordination. Focus on aligning manufacturing, analytical development, quality assurance, regulatory affairs, and commercial stakeholders while tracking milestones, resources, budgets, and execution across a regulated product lifecycle.
Location: Hybrid role based in Bridgewater, New Jersey, United States, with remote work most of the time and in-person collaboration as needed. Frequent domestic and international travel of up to 20% is required.
Company
Global biopharmaceutical company focused on developing treatments that transform the lives of patients with serious and rare diseases.
What you will do
- Lead internal and external project teams across research, development, regulatory submission, launch, and post-launch lifecycle management.
- Align Manufacturing, Analytical Development, Quality Assurance, Regulatory Affairs, Commercial, Research, and Clinical functions around shared project goals.
- Establish project frameworks covering roles, deliverables, decision-making, milestones, communication, and governance.
- Identify risks and opportunities, develop mitigation strategies, and escalate critical issues for timely decisions.
- Deploy project management tools, visuals, and metrics to improve planning, execution, visibility, and accountability.
- Coordinate with CDMOs and external partners while supporting budget planning and resource forecasting.
Requirements
- Bachelor’s degree and five years of experience in the pharmaceutical, biotech, or medical device industry.
- Experience leading cross-functional teams and driving accountability without direct authority.
- Experience managing projects across the product lifecycle from development through launch.
- Strong communication, collaboration, organizational, and project planning skills.
- Proficiency with MS Project, Excel, PowerPoint, SharePoint, or Smartsheet.
- Ability to work effectively in fast-paced, regulated environments.
Nice to have
- PMP certification.
- Working knowledge of research, clinical, regulatory, manufacturing, and quality processes across drug development.
- Entrepreneurial mindset and continuous improvement orientation.
Culture & Benefits
- Hybrid work model with flexible schedules and purposeful in-person collaboration.
- Medical, dental, vision, and mental health support, plus an annual wellbeing reimbursement and Employee Assistance Program.
- Paid time off, fertility and family-forming benefits, caregiver support, and company-paid life and disability insurance.
- 401(k) company match, annual equity awards, and Employee Stock Purchase Plan participation.
- Learning programs, LinkedIn Learning, workshops, mentorship, employee resource groups, and volunteer opportunities.
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