2 дня назад
Project Manager (CapEx Qualification & Infrastructure, Filtration, Med. Device)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Project Manager (CapEx Qualification & Infrastructure, Filtration, Med. Device) (Manufacturing Capital Projects): Leading and delivering strategic manufacturing capital, infrastructure, process improvement, and equipment projects in a regulated life sciences environment with an accent on safety, quality, schedule, budget, and compliance. Focus on managing complex cross-functional initiatives, preparing CapEx justifications and financial analyses, and coordinating qualification, validation, and change-control activities.
Location: On-site in Pensacola, Florida, United States; up to 15% potentially international travel.
Company
’s Cytiva operating company develops solutions for life sciences, diagnostics, biotechnology, vaccines, medicines, and cell and gene therapies.
What you will do
- Lead the planning, execution, monitoring, and closure of manufacturing projects using project management methodologies and Business System principles.
- Deliver capital, infrastructure, equipment, process improvement, and operational projects safely, on schedule, within scope and budget, and in compliance with quality and regulatory requirements.
- Manage project scope, change control, risks, schedules, resources, and budget impacts across multiple concurrent projects.
- Maintain communication with senior leadership and operational stakeholders on project status, risks, mitigation plans, and business outcomes.
- Prepare CapEx justifications, financial analyses, budget forecasts, return-on-investment analyses, and executive presentations.
Requirements
- Bachelor’s degree.
- Preferred: 3+ years of experience managing large-scale manufacturing, facility, infrastructure, or equipment projects, including budgets exceeding $10 million.
- Experience leading complex cross-functional projects in manufacturing, engineering, life sciences, medical device, pharmaceutical, biotechnology, or related regulated industries.
- Strong knowledge of scope management, scheduling, budgeting, resource planning, risk management, and stakeholder management.
- Strong financial acumen in capital planning, forecasting, return-on-investment analysis, and cost control.
- Ability to work in an on-site manufacturing environment and follow safety protocols and procedures.
Nice to have
- Experience with Management of Change processes in regulated manufacturing environments.
- Experience commissioning, qualifying, and validating manufacturing equipment and facilities.
- Experience in pharmaceutical, biotechnology, medical device, or life sciences manufacturing operations.
Culture & Benefits
- Culture focused on belonging, continuous improvement, and life sciences innovation.
- Paid time off.
- Medical, dental, and vision insurance for eligible employees.
- 401(k) for eligible employees.
- Eligibility for bonus or incentive pay.
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