Director, Global Apheresis Operations
vor 2 Wochen
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.
You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity.
Take your career farther than you thought possible.Summary:
Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today.
With therapies only in their infancy and BMS's continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.
The Director, Global Apheresis Operations is accountable for the network of global collection centers used to support BMS Clinical and Commercial Cell Therapies and the BMS teams responsible for the onboarding and management of these centers.
This role will be based out of the corporate offices in Seattle WA or Boudry, Switzerland and will report to the Executive Director of Global Patient Operations located in Seattle, WA.
Responsibilities:
- Lead the global program and team of 20+ that builds and manages the network of cell collection centers that support BMS Clinical and Commercial Cell Therapy products.
- Responsible for the existing regionally based teams in North America, Europe and Japan and for ensuring capabilities exist to build and maintain collection center networks in new markets.
- Identify, implement and manage strategic partnerships to increase scale for Apheresis site onboarding and management.
- Work with Patient Operations Project Management Team to ensure plans are developed and tracked for all major projects including but not limited to commercial launches, new product introductions and major changes/updates to existing procedures, protocols and systems.
- Partner closely with Global Head of Scheduling and Cell Logistics to ensure alignment on processes, communication, and customer experience.
- Ensure alignment with Commercial, Clinical and Quality on global site qualification plans.
- Accountable for ensuring teams work with other global Cell Therapy Leads in Quality and MSAT to ensure collection protocols are compliant and maintained.
- Ensure roles and responsibilities and accountabilities are clearly defined across all regional teams
- Manage departmental budget and ensure adherence to the approved budget and forecasts.
- Accountable for reporting global quarterly KPI's and metrics and implementation of global process improvement system.
- Responsible for maintenance and improvement of global policies, procedures and systems.
- Ensure process is implemented to clearly identify and manage global versus regional requirements.
- Ensure global customer feedback program is implemented to support continuous improvement.
- Chair the Apheresis Operations functional governance meeting and represent the Apheresis Operations team on global program teams, as required.
- Draft relevant sections of global regulatory filings and ensure global Apheresis Operations team is prepared to support regulatory audits, as required.
- Foster team health and engagement, motivate people, and resolve problems that prevent teams from succeeding—especially in an extremely fastpaced continuously changing environment.
Qualifications:
- Undergraduate Degree in Life Sciences, minimum 10 years of pharmaceutical or biotech GMP operations or supply chain experience, including clinical and commercial
- Minimum 5 years' experience working in autologous cellular therapy, Apheresis or Stem Cell Transplant programs
- Minimum 5 years of management experience, with experience building teams, and with coaching and managing people managers; experience with global team
- Excellent working knowledge of FDA and international regulatory requirements for biologics and cells/tissue
- Demonstrated excellent leadership, communication and presentation skills
- Independently motivated, detail oriented and good problemsolving ability
- Highly collaborative team player who fosters open communication and facilitates mutual understanding and cooperation between all stakeholders
- Ability to navigate and be successful in a fastpaced, highlymatrixed work environment
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