4 дня назад
Manager, Project Management – Technical Operations (Biotech)
124 000 - 161 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
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
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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