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Under the guidance of senior staff, supervisor, or trainer, capable of performing manufacturing processes and following current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and data integrity practices within a cleanroom environment.
$75,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Battery Engineer/Scientist - Lithium-Ion Battery Manufacturing - San Diego. I'm looking for some talented Battery Manufacturing Engineer/Scientists with strong backgrounds working in Li-ion battery manufacturing and next-gen battery cell technology to join my client as they begin to ramp up production.
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The ideal candidate will also have experience with Blow-Fill-Seal (BFS) manufacturing, supporting CMC regulatory submissions, managing statistical analysis tools for trending stability data, and providing experienced technical support of GMP operations at CMO’s as Person-In-Plant all while working in a high-paced environment to deliver innovative therapies to patients in need.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Pharmaceutical expertise includes Oral Solid Dosage, Semi-Solids, Liquid-Dosage (TS and Aseptic), API manufacturing, Biotechnology (Vaccines, Blood Plasma Fractions, Monoclonal Antibodies). This role is for Bioprocess C&Q Engineer role to work on the commissioning, qualification, startup of upstream and downstream bioprocess systems/equipment in the biopharmaceutical industry, as well as process equipment in pharma/biotech industries.
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The Manufacturing Infrastructure Support Technician position will join a new team dedicated to develop, support, maintain and troubleshoot problems related to the manufacturing IT / OT environments across the Saint Gobain North American facilities.
$120,100 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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A Manufacturing Technician 1 must be able to perform a wide variety of essential functions across multiple manufacturing work centers including assembly packaging and alight industrial work.
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Ensure clear communication to Company’s senior management on the status of clinical inventory, manufacturing projects and goals as they relate to cross-functional business success. Lead CMC operations focusing on all areas including but not limited to GMP manufacturing, facility management, procurement, biologics process development, regulatory documentation, validation and change control and supply chain management.
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The Process Development Engineer will work to design, develop, and implement, new and improved manufacturing processes for the company's control console program. Experience in Design for Manufacturing (DFM), Lean Manufacturing, Design of Experiments (DoE), technology/process transfer experience, product/process failure mode and effects analysis (FMEA), and problem solving methodologies.
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Innovive is a consistently growing B2B manufacturing company serving the biomedical research industry. Demonstrated ability to develop comprehensive manufacturing and fabrication documentation.
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Under general supervision, the Manufacturing Associate, Downstream, will perform routine manufacturing activities in GMP manufacturing areas including purification and the associated sub-processes/ preparation.
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Experience with at least one of the following preferred: moving, warehouse, manufacturing, inventory management, stocking, customer service, helper or general labor. Iron Mountain helps lower cost and risk, comply with regulations, recover from disaster, and enable digital and sustainable solutions, whether in information management, digital transformation, secure storage and destruction, data center operations, cloud services, or art storage and logistics.
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The Associate Director of AOC Process Development and Manufacturing - Bioconjugation is a senior leader accountable for managing all aspects of AOC drug substance (DS) process development and manufacturing, including the scale-up to Phase 3 and commercial.
$194,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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This role shall daily exercise and build a foundation of ERP (Enterprise Resource Planning), MRP (Material Resource Planning), and manufacturing transaction process best practices pertaining to Regulation (EU – MDD & MDR, cGMP (current Good Manufacturing Practice), and other country specific regulations.
$100,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Develop manufacturing plans with resources and supervise schedules to meet clinical demand and new clinical trials on both the cell therapy and/or exosome platforms. 8+ years of hands-on cGMP biologics manufacturing experience in pharmaceutical/biotech industry.
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Use your hands-on knowledge and skills to participate in multiple phases of our Engineering/Manufacturing Design & Development process. Ability to work in an office and manufacturing environment (Constant.
InternExpandApply NowActive JobUpdated 4 days ago
manufacturing job Title: engineer senior Company: Kyocera in San Diego, CA
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