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The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners.
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Job DescriptionDirector, R&D Quality, GCP - Cell Gene Therapy (CGT)The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners and supports the program and study level quality leads in key quality related clinical activities and deliverables for all CGT programs across the Vertex clinical portfolio.
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The Strategic Sourcing Supply Chain lead will own Category Management activities across Vertex for distribution, logistics, and warehousing for complex supply chains involving small molecule, biologics and Cell and Gene Therapy products.
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This client is a growing international full-service CDMO/CRO within the biotechnology space looking to aggressively expand its footprint in the US. The company has a strong base of API/Small Molecule, Biologics, Clinical Research, Bioanalytical Sciences, DMPK, Cell and Gene Therapy and other capability centers across the US. This business has developed a fantastic brand in the US through exceptional service which drives repeat business.
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Executive Director, Immunology Cell Therapy Translational Science - Permanent - Boston MA. Proclinical are seeking an innovative leader in translational science to head up the Immunology Cell Therapy Translational Science team.
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Associate Director, BaseCamp Business Development ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine.
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Experience in cell and gene therapy. Providing advice on regulatory issues for both marketed and pipeline products; actively collaborates with management, Global Regulatory Lead and cross functional colleagues within Alexion (i.e., commercial, research, clinical development, medical affairs, business development, legal, manufacturing, quality, portfolio management, financial, human resources, etc.
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This role will be responsible for driving translational and biomarker activities in a biopharma company building a leading portfolio of cell therapies for immunology and autoimmune diseases. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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Lead development and execution of the commercial and business strategy in the Cell Therapy Franchise. Acts as day to day commercial and business escalation for Cell Therapy within RESILIENCE, serves active role in governance of customer relationships and site on respective PAD and manufacturing SLT (s.
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Our Patient Supply Team is hiring an Associate Director, Supply Chain Planning to be a Business Process Owner for Sales & Operations (S&OP) Planning process and responsible for managing end to end commercial process for cell & gene therapy.
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We are now recruiting a Director, Clinical Regulatory Writing (CReW), Immunology Cell Therapy Program Lead. In this role you will provide expert leadership to the delivery of the product pipeline through partnering with senior leaders to define and lead the global communications strategy.
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We provide biomanufacturing strategy and execution to start up and established gene and cell therapy, pharmaceutical, and biotechnology companies. The Director Project Controls plays a strategic leadership role with relentless focus on Business Development and organizational growth while ensuring Project Delivery via their own billability, as well as, training, mentoring, and coaching their teams in both the evolution and continued operational excellence of Precision for Medicine's Manufacturing Solutions practice area.
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This role will specifically focus on driving growth in healthcare and biotechnologies related businesses including gene & cell therapy manufacturing, regenerative medicine and medical foods within the AJINOMOTO Group.
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Strong knowledge of US drug development and regulatory policy; excellent scientific and business judgment. Monitoring the development of new regulatory requirements or guidance documents and advising product teams of the impact on the business or development programs.
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Director, Global Regulatory Affairs, Development Strategy. Representing Alexion as point contact FDA and leading Alexion delegation for regulatory authority meetings. Developing and directing innovative and effective regulatory strategies in support of specific projects, and across projects in the Alexion portfolio.
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business cell therapy jobs Title: director in Cambridge, MA
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