Director, Global Regulatory Sciences Liaison, Cell Therapy, Hematology or Oncology
vor 3 Monaten
Assures that organization follows through to achieve high quality execution of plans.Ability to contribute and add value to the writing of scientific documents for regulatory purpose.Able to act as Contact Person for assigned project(s) with EMA in line with BMS strategy and to provide strategic directions and supervise negotiations with other relevant regulatory agencies for assigned project.Provides direction for maximizing opportunities within projects (eg. lifecycle) and across the geographical area to support the productivity priorities.Participates actively in and represents GRS-EU for their project(s) in the Global Regulatory Team and on various multi-functional committees or teams.Communicates actively and timely with Global Regulatory Sciences colleagues in European countries, including through direction of European Regulatory Teams.Active participation in regional organizational activities for the Liaison function (across projects)Develops strong working relationships with key stakeholders both within and outside the company.Builds and maintains strong relationships with alliance partner when applicable.Watches, anticipates and acts on trends and changes in the European and international regulatory environment which may impact on the business.Integrates the European regulatory, legal, scientific/medical and business perspectives to achieve the optimal regulatory outcomes for assigned project(s) in accordance with company objectives.Qualifications, Knowledge and Skills Required:Strong scientific/medical background.Understanding of pharmaceutical product developmentUnderstanding of European regulatory principles and their impact on company’s development and businessUnderstanding of the complexities of cross functional management issuesUnderstanding of legal and business aspects related to European regulatory procedures and outcomes.Conducted prior negotiations with (a) regulatory authority(ies)Contributed to scientific documents developed for regulatory purpose.Established credibility and respect during previous exposure with regulatory authorities and peersDemonstrated ability to react appropriately in difficult, possibly adverse, conditions and/or in crisis situationsDemonstrated ability to integrate regulatory, scientific/medical and business perspectives and to translate this analysis into practical recommendations and operational goalsDeveloped
working relationships and/or build a team resulting in a performant network or organizationDemonstrated values, behaviors, professional standards and cultural sensitivity compatible with BMS vision and culture.Why you should applyYou will help patients in their fight against serious diseases You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees. You’ll get a competitive salary and a great benefits package Bristol Myers Squibb has been certified as a Great Place to Work in Switzerland Each day, our collaborative teams come together to support some of the most interesting work of their careers. For more information about Bristol Myers Squibb, visit us at #LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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Director, Regulatory Cmc
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Director, Global Regulatory Lead
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Cell Therapy Process Engineer
vor 4 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitUnlock the Future of Cell TherapyBristol Myers Squibb is reimagining the future of cell therapy, and we're looking for a talented individual to join our team as a Cell Therapy Process Engineer. As a key member of our Cell Therapy team, you will play a critical role in supporting the production of personalized cell therapy products at Contract Manufacturing...
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Director, Global Regulatory Lead, Oncology
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Director, Cell Therapy, Medical Communications
vor 6 Monaten
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Cell Therapy Manufacturing Specialist
vor 1 Monat
Boudry District, Schweiz Bristol Myers Squibb VollzeitUnlock the Future of Cell TherapyBristol Myers Squibb is at the forefront of revolutionizing the field of cell therapy. As a key player in this exciting space, we are seeking a highly skilled and experienced professional to join our team as a Cell Therapy Manufacturing Specialist.Key Responsibilities:Provide technical support to manufacturing teams to ensure...
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Director, Global Apheresis Operations
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Associate Director, Global Regulatory Science
vor 5 Monaten
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Director, Global Operations, Scheduling and Cell
vor 4 Monaten
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Cell Therapy Process Engineer
vor 1 Woche
Boudry District, Schweiz Bristol Myers Squibb VollzeitUnlock the Future of Cell TherapyBristol Myers Squibb is at the forefront of revolutionizing the field of cell therapy. As a leading biopharmaceutical company, we are committed to delivering innovative solutions that transform the lives of patients. We are seeking a highly skilled and experienced professional to join our team as a Cell Therapy Process...
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Associate Director, Global Regulatory Strategy
vor 4 Monaten
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Vp, Late Clinical Development Oncology
vor 5 Monaten
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Director, Ww Medical Cell Therapy, Lymphoma
vor 5 Monaten
Boudry, Schweiz Bristol-Myers Squibb Vollzeit**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...
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Director, Global Regulatory Lead
vor 4 Monaten
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Director, Ww Medical Affairs, Cell Therapy
vor 4 Monaten
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Associate Director Cell Therapy QA External Drug
vor 5 Monaten
Boudry, Schweiz Bristol-Myers Squibb Vollzeit**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...
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Associate Director Cell Therapy QA External Drug
vor 5 Monaten
Boudry, Schweiz Bristol-Myers Squibb Vollzeit**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...
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Cell Therapy Production Manager
vor 2 Monaten
Boudry District, Schweiz Bristol Myers Squibb VollzeitJob SummaryBristol Myers Squibb is seeking a highly skilled and experienced professional to join our team as a Senior Manager of Cell Therapy Manufacturing. This role will be responsible for supporting the production of personalized cell therapy products at Contract Manufacturing Organizations (CMOs) for both global clinical trials and commercial supply.Key...
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Boudry District, Schweiz Bristol Myers Squibb VollzeitTransforming Lives through Medical EducationBristol Myers Squibb is a place where innovation meets impact. As a leading biopharmaceutical company, we're committed to transforming lives through our groundbreaking work in cell therapy and medical education. We're seeking an exceptional Associate Director to join our team and contribute to our mission.Key...
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Vice President, Cell Therapy External Manufacturing
vor 5 Monaten
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