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We are looking for a motivated Corporate Counsel – Cell Site Leasing to provide legal counsel and support negotiations with landlord entities through the T-Mobile network siting and construction process.
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If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team. Proven record with the successful implementation and management of the Quality System in a sterile, biologics or cell therapy commercial manufacturing facility.
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We are committed to creating a diverse workforce that embodies a deep culture of acceptance, equity, and inclusion. The Wonderful Sales Merchandiser role is responsible to increase brand awareness for the grocery store shopper promoting some of the most known household brands.
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The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing.
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR part 11 electronic records and electronic signatures, and good documentation practices with the ALCOA+ principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles.
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The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES team to create, manage, and improve computerized systems/Recipes validation deliverables for electronic systems, applications, and associated controls to maintain data integrity supporting ALCOA+ principles throughout the CSV lifecycle.
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Familiar with the development of CSV documentation (Validation Plans, Requirements, Design / Configuration Specifications, Test Scripts [IQ / OQ / PQ / UAT], Summary Reports, Trace Matrices, SOPs). Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR Part 11 electronic records and electronic signatures, and good documentation practices with the Client principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles.
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Title: Validation - Specialist, MSEO Manufacturing Systems Validation. Minimum of 2+ years relevant work experience required preferably in a pharmaceutical manufacturing environment. The Specialist will be responsible for ensuring the validation of the S12 Enterprise Manufacturing Execution System (EMES), and applications are done following the relevant Client procedures, such as CSV SOP but no limited and applicable health authority regulations.
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At Bristol Myers Squibb we are reimagining the future of cell therapy. General understanding of cGMP, ISO, FDA, MHRA, PMDA, USP, ATMP, PDA and EP regulations and guidelines as related to the manufactured of cell therapy products.
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Partner with other members the Cell Therapy Operations Training Team and other training teams across the organization to build harmony and alignment. Align, coach, and develop training programs that drive an increase in overall training effectiveness and the empowerment Cell Therapy personnel.
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We understand that diversity, equity, and inclusion are essential elements to our work and are vital to the organizational culture and programmatic success of MSU Extension. We embrace that it is everyone’s job to create a culture that promotes diversity, equity, inclusion and belonging.
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Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique. Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
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At Ports America, the Learning & Development Manager is responsible for supporting the company strategy to drive a high-performance learning culture. Partner with leadership to develop a learning culture across the organization that cultivates an engaged workforce, supports our company culture and results in reduced turnover.
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Through the model of Shared Governance, collaborate with all members of the health care team with a focus on promoting evidenced based care within a healing culture for the patient population served and their families.
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Basic knowledge of cGMP’s and multi-national biopharmaceutical/cell therapy regulations. Reports to Associate Director, Manufacturing Science & Technology (MSAT), Cell Therapy. Work scope will include commercial manufacturing and clinical manufacturing for all cell therapy products manufactured in Summit, NJ Building S12.
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