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4 дня назад

Manager, Project Management – Technical Operations (Biotech)

124 000 - 161 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
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
Manager, Project Management – Technical Operations (Biotech): Driving complex pharmaceutical and biotech pipeline projects from research transition through development, regulatory submission, launch, and post-launch lifecycle management with an accent on cross-functional CMC leadership, project planning, and external partner coordination. Focus on integrating manufacturing, analytical development, quality assurance, and regulatory affairs, managing project risks, and maintaining delivery alignment in a regulated environment.

Location: Hybrid role based out of the [City, Country] office, with remote work available most of the time and in-person collaboration when needed. Frequent domestic and/or international travel of up to 20% is required.

Salary: $124,000–$161,000 annual

Company

hirify.global is a global biopharmaceutical company focused on transforming the lives of patients with serious and rare diseases.

What you will do

  • Lead complex pipeline projects from research transition through development, regulatory submission, commercial launch, and post-launch lifecycle management.
  • Lead cross-functional Chemistry, Manufacturing & Controls teams and coordinate internal departments and external partners.
  • Align Manufacturing, Analytical Development, Quality Assurance, Regulatory Affairs, Commercial, Research, and Clinical stakeholders around project goals.
  • Establish project frameworks, define responsibilities and deliverables, track milestones, and communicate progress to teams and leadership.
  • Identify risks and opportunities, develop mitigation strategies, escalate critical issues, and support timely decision-making.
  • Support budget planning, resource forecasting, project management tools, governance forums, and relationships with CDMOs.

Requirements

  • Bachelor’s degree and at least 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 project management tools such as MS Project, Excel, PowerPoint, SharePoint, and Smartsheet.
  • Ability to adapt and work effectively in fast-paced, regulated environments.

Nice to have

  • PMP certification.
  • Working knowledge of the full drug development process, including Research, Clinical, Regulatory, Manufacturing, and Quality.
  • Entrepreneurial mindset and continuous improvement orientation.

Culture & Benefits

  • People-centered culture focused on meaningful progress for patients and continuous improvement.
  • Medical, dental, and vision coverage, mental health support, wellbeing reimbursement, and Employee Assistance Program access.
  • Paid time off, fertility and family-forming benefits, caregiver support, and flexible work schedules.
  • 401(k) with company match, annual equity awards, ESPP participation, and company-paid life and disability insurance.
  • Learning programs, LinkedIn Learning, workshops, leadership development, mentorship, networking, employee resource groups, and service opportunities.

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