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Process Engineer Position Summary:Catalent Pharma Solutions is Chelsea, MA is hiring a Process Engineer who is responsible for assisting senior engineering staff in the design and implementation of manufacturing processes, instrumentation and equipment for clinical and commercial manufacturing.
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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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Act as the key contact to SQF practitioner, OSHA and for all plant manufacturing practices & maintenance. Contact: John@SourceRecruitmentSolutions.com Our client, a premier Food Manufacturing Company with products sold nation wide is seeking an experienced Quality Assurance Manager.
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Prior experience must include: Perform purification process, including experimental planning, sample handling, method creation; Conduct tech transfer for manufacturing sites; Analyze experimental data using JMP; Write technical documents; Monitor GMP manufacturing and related in-process controls; Implement new technology associated with continuous processing; Develop and transfer methods (purification process & analytical.
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Familiarity with the manufacturing industry - process engineering, manufacturing engineering, and related experience a significant plus. Companies of all sizes, across industries including consumer electronics, aerospace and defense, contract manufacturing, automotive, apparel, medical devices and more, have implemented Tulip's intuitive platform to solve some of the most pressing challenges in manufacturing: error-proofing processes with guided workflows, integrating industrial edge technologies with legacy factory machines, and capturing and analyzing real-time production floor data.
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This position leads various teams within FMI, directing quality personnel working with manufacturing and IVD operations teams within the Quality System Program, including manufacturing process review, batch release of products, IVD assay validation and verification, manufacturing material acceptance, device non-conformance and CAPA investigation.
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Our core mechanical competencies span precision fabrication, diamond turning, EDM machining, additive manufacturing, and 5-axis machining. Requirements: 3 years of experience applicable experience required in both milling and turning subtractive manufacturing technologies (manual and CNC) Competency in reading a mechanical drawing and basic understanding of GD&T Ability to design and fabricate basic fixtures Experience using basic hand tools and inspection equipment, such as: Calipers, thread/pin gages, micrometers, dial indicator, etc.
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Minimum of 5 years experience in developing, building, and testing complex electro-mechanical medical devices, design transfer, and process validation with broad knowledge of electrical, mechatronics, firmware, software, and systems engineering, including design verification testing, and transfer to manufacturing within a regulated medical device development environment.
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Serve as the Quality SME on the Chemistry, Manufacturing, and Controls (CMC) Governance teams covering Analytical Development, Process Development, Technical Operations, and Supply Chain topics for technical transfers, new product introduction, clinical trial and commercial products to assure a compliant strategy is developed, executed and maintained.
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Tecogen Inc. has an immediate opening for a full time Engine Mechanical Assembly Technician located in Waltham, MA to work in our manufacturing facility. Manufacturing Technicians are provided will all necessary tools.
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ERM is seeking a mid-level Demolition & Environmental Remediation Project Engineer to join our top-ranked global environmental consulting firm in Boston, MA. As part of a growing and diverse local office, you will work on complex site, remediation and environmental construction projects at a variety of oil & gas, industrial manufacturing, and power plant sites across North America.
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The Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is accountable for executing global CMC regulatory strategies for our programs in early and late-stage development through and beyond approval.
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Fusion Optix is seeking a highly skilled and detail-oriented Quality Technician to join our Assembly Group responsible for manufacturing specification grade LED lighting products. Proven experience as a Quality Technician or similar role in a manufacturing environment, preferably in the production of LED lighting products or electronics.
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The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp®, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
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Vestas is the world's largest wind turbine manufacturing company with significant operations in the United States. 5 or more years of work experience in the offshore (wind) construction, maritime, or marine industries with a strong preference for time working on vessels or in shipyards.
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manufacturing job Title: process engineer Company: Crh in Cambridge, MA
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