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Support tech transfer of new products and processes to ensure smooth transition from process development/clients into GMP manufacturing. Participating in start-up efforts of new equipment, software or processes in manufacturing.
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In this role, you'll be responsible for designing power systems that deliver power to automated manufacturing processes and assisting in the electrical design of new manufacturing buildings.
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We currently have an opportunity for a scientist to join our team in Varicella bulk vaccine manufacturing, supporting a new PAT (process analytical technology) lab and laboratory operations.
$22 - $24 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Senior Quality Engineer will support our new manufacturing plant in King of Prussia, Pa focusing on continuous improvement in quality, process control, material efficiency, and start-up of a new GMP manufacturing plant.
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Does this person have experience working on CMC (Chemistry Manufacturing and Control) or Safety/DMPK aspects of pharmaceutical products as a workstream/technical lead? Note the following does NOT fit the requirement: management of clinical trials, IT project management, facilities project management or project management within a Pharma company but hasn’t supported development/project management of a new medicine.
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As a Sr. Safety Engineer, you will be responsible for the onsite safety of Upper Merion and Upper Providence R&D manufacturing areas by ensuring adherence to site safety programs and GSK standards, complying with process safety requirements, leading safety investigations, and continuously improving the site’s safety culture.
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Assists in determining capacity and production standards •Estimates and validates production capacity via pilot builds and run at rate studies to establish labor content of end items •Develops process change plans, validates change effectiveness and implements changes in processes, time standards and bills of material •Coordinates Tool Room, Suppliers, Machine Shop and Maintenance in the design and development of new tooling, fixtures, nests, machinery and controls.
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This team is responsible for setting up an entire new manufacturing operation for syringe and vial filing. Developing and implementing manufacturing processes for new products and overseeing all project scheduling.
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This role works closely with the Chemistry, Manufacturing and Controls (CMC), Regulatory Affairs, and Quality Assurance departments, as well as with cross-functional project teams. Manages a CMC team who manage relevant submissions to US investigational new drug applications (IND), ex-US clinical trial applications, and new drug applications (NDAs.
$188,500 - $269,250 a yearFull-timeExpandUpdated 14 days ago - UpvoteDownvoteShare Job
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The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and.
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Coordinate onboarding activities for new MRs including training, weekly communications, co-ordination of low margin jobs, quoting and order management activities, account visits and sales ride-along calls.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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2-4 years’ Experience in Validating SAP systems in Manufacturing Experienced in CSV activities in Manufacturing related applications like SAP Systems, Product Serialization systems, MES systems Perform review for GxP systems to ensure compliance with regulatory requirements.
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The Senior Manager, Quality Control Analytical will partner with Analytical Development to coordinate the transfer and qualification/validation of new assays in the QC Analytical Laboratory. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
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As a Production Technician at Purolite, an Ecolab Company, you will join our operations team at our new Life sciences manufacturing facility in King of Prussia, PA. This is a great opportunity to join and advance with an innovative and high-growth global company committed to sustainability.
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Proficient in Discrete & Lean Manufacturing, Product Data Management, Inventory Management, Shop Floor Management, Forecasting, Demand Planning, MRP & MPS, Material & Capacity Planning, Product Costing & Manufacturing Accounting, Quality Management, Procurement.
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