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We are seeking a highly motivated Director of MSAT who will be responsible for supporting the launch, ramp-up, and production activities within a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to manufacture autologous and allogeneic cell therapy products.
$170,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Working at the intersection of automation engineering, computational design and polymer science, we design and commercially manufacture highly customizable materials and products- everything from medical devices to luxury fashion.
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We also manufacture extruded seamless pipe, fittings, and forgings for power generation and oil & gas applications; commercial and military airframe aerostructures; and metal alloys and other materials for the casting and forging industries.
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Working with CMC stakeholders and external providers of GMP goods and services (CDMOs), provide independent tactical quality expertise for external manufacturing and distribution programs and oversee the GMP activities supporting material receipt, drug substance, intermediate, and bulk drug product manufacture, packaging and labeling, and batch review and disposition at Rivus CDMOs.
$200,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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At Jushi Holdings Inc. ”) ( CSE: JUSH ) ( OTCQX: JUSHF ), we are shaping the future of the cannabis industry, the fastest-growing jobs sector in the U.S. The Director of Processing will be responsible for leading the Processing Department at Jushi’s Scranton, PA facility.
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Backed by some of the world's top venture capital firms, we design and manufacture electrolytic hydrogen systems matched to renewable power sources to create green hydrogen by splitting water. We are searching for a Director of Service Engineering to be responsible for after-sales support for all globally deployed electrolyzer systems.
$208,000 - $229,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Reports directly to Site Operations Leader or Site Engineering Leader, dotted to Continuous Improvement Director. We manufacture and distribute nutritional, pharmaceutical, personal care, facial care, home hygiene, and other wellness products and distribute them directly to the consumer through a full-service catalog and Internet shopping system.
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Job Description: Lilly is currently constructing a cutting-edge facility for the manufacture of new modalities including Gene Therapy. Additionally, the Associate Director will oversee performance consulting for business partners to assess critical business needs and recommend learning solutions that address capability and competency gaps.
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Maintain facilities adequate to ensure the manufacture of products to requirements and for the storage and handling of raw materials, WIP and finished goods. Provide direct supervision to Production Control Manager, Manufacturing Supervisor, and Lead personnel as well as the Maintenance Supervisor Ensure a comprehensive continuous improvement program to achieve operational excellence throughout the organization.
$80,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a Senior Director Gene Editing Technologies within the Analytical Development department, you will report to the Vice President Head of Analytical Development and lead a function accountable for establishing deep characterization and knowledge of gene editing technologies used in the manufacture Sana’s cell therapy products.
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The Director of Manufacturing is responsible for activities related to the manufacture and production of electronic and electro-mechanical assemblies incorporated in industrial radios, achieving delivery, quality, and cost targets.
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Rite-Hite is the global leader in the manufacture and distribution of industrial loading dock and door equipment. The manager of FP&A will report directly to the Director Financial Planning & Analysis.
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You will report to the Associate Engineering Director - Automation Manufacturing in Social Circle, GA. You will be a part of the Automation Engineering Team. The Automation Engineering Team ensures that the manufacturing equipment/systems and Automation systems used in the manufacture, storage, testing, and distribution of Takeda products are fit for purpose following Takeda standards and industry regulatory requirements.
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The pilot plant’s mission is to serve as PR&D’s internal node for small molecule drug substance clinical manufacture, and as preferred site for first pilot of commercial small molecule processes, enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing.
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This individual will partner with the SVP of Operations and EVP of Commercialization to expand Cellares' US and Global footprint and shape effective collaborations with Small to Large Pharma/Biotech partners to manufacture world-class cell therapy products.
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