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Advanced degree (BS, MS or PhD) in Chemical/Biochemical Engineering, Biochemistry, Immunology, or related degree with experience (8+ for BS, 5+ for MS, 2+ for PhD) in process development and manufacturing sciences in cell therapy, biotechnology, or pharmaceutical industry.
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The position focuses on process improvement related to clinical care, patient access, staffing, utilization management, and patient scheduling. Additional responsibilities include contributing to the development, implementation, and monitoring of quality improvement and compliance initiatives, as well as involvement in budgeting and strategic planning.
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Provide leadership and coordination for the development and implementation of a cohesive approach to measuring and promoting quality and lead priority-setting process for clinical quality improvement for MassHealth’s payment and care delivery innovation initiatives, including ACOs, MCOs and CPs.
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Continuous Improvement: Identify process and control gaps and champion improvement initiatives through Practical Process Improvement (PPI) The Senior Sales Compensation Analyst will partner with the Director, Sales Operations in supporting the Pharma Services Group (PSG) Global Sales organization compensation process.
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Experience with process optimization, lean manufacturing, and continuous improvement methodologies. Drive a culture of continuous improvement, encouraging the identification and implementation of process enhancements.
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5 years of post graduate experience in project management and leading workstreams; execution of finance transformation, FP&A, and/or business process design/improvement initiatives; strong understanding of financial and accounting systems; deep knowledge in finance best practices and governance; demonstrable expertise in process improvement and organizational design.
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Director/Sr. Director - Process DevelopmentGreater Boston Area Competitive Compensation + excellent bonus/benefitsDuties and Responsibilities:Lead all process development activities (cell culture/banking/development, fermentation, protein purification, tech transfers)Oversee internal(in-house) and external vendors (domestic & international CDMOs)Work cross-functionally with CMC & Manufacturing leaders such as Analytical, Drug Product, QA/QC, Manufacturing, Supply Chain, etc.
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Along with the CLIA Lab Director and leadership, maintain laboratory audit readiness by overseeing and managing clinical lab audits with regulators, pharmaceutical partners, and with other agencies, ensuring that internal system and process audits are scheduled and conducted.
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Continued process improvement and support for the creation of a new best-in-class crypto booking system. 0-3 years’ investment operations or corporate actions experience within a recognised Tier 1 or 2 financial services environment (good internships and crypto specific college courses will be considered for candidates with less than 1 year experience postgraduation.
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This position is a multi-faceted role including supervising and coordinating the processing of Accounts Payable expense activities, supporting process improvement projects and will be under the direction of Accounts Payable Manager.
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Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services. CAPS is part of the B. Braun Group of Companies in the U.S.
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Non-Viral Delivery Process Development Co-op. Contribute to and execute, study design for lipid nanoparticle process development, process scale-up and final product characterization.
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Amgen is currently seeking a talented Process Development Senior Associate to join our Drug Substance Technologies - Synthetics (DSTS) group in Cambridge, MA. Amgens DSTS group within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets.
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The incumbent will provide Automation support to the daily operations, continuous improvement, and projects for the Pilot Plant, Bulk Manufacturing, Filling, Assembly, Packaging, Utilities, Facilities, and other DCS and PLC Automated Equipment and Control Systems on a GMP regulated environment.
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Contribute to the quality management of the Drug Safety system, ensuring department standards are met and implementing continuous improvement actions. Senior Drug Safety Specialist, Pharmacovigilance Records & Compliance 2022831.
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process improvement jobs Title: process coordinator Company: Pearson in Boston, MA
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