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At least 2 years’ experience in Quality Assurance, Microbiology, Sterile Compounding in pharmaceutical manufacturing. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide.
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We are currently recruiting a Process Engineer I who will be part of a growing engineering organization supporting all groups within the Vector Program in addition to our cGMP manufacturing team.
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Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical and biotechnology industries.
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Must have a demonstrated record of accomplishment in a manufacturing culture focused on safety, reliability, and process improvement. The Sr. Process Engineer plans and manages capital growth, maintenance, and process-related improvement projects associated with US Silica operations.
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The Microelectronics Process Engineer will lead and support microelectronics manufacturing projects at all levels of integration: die/wafer, component level packaging, multi-chip module (MCM), printed circuit board (PCB), and system level packaging.
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Experience as a project team leader performing RCA, process improvement teams. If so, Georgia-Pacific has an opportunity for a talented Process Engineer at our Palatka Pulp and Paper Manufacturing operation.
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5 years + experience in process optimization, operations, or business management in manufacturing. Job DescriptionTitle: Continuous Improvement ManagerWho We Are:Carboline is a St. Louis-based coatings manufacturer with a global reach.
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The Manufacturing Engineer is responsible for the planning, coordination, and execution of new process development, continuous improvement projects, and other technical tasks as needed.
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Solid working knowledge of various manufacturing platforms (Microbial fermentation process, IB recovery and refolding, CHO cell culture and purification, Pegylation, PEGylated protein purification etc.
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Reporting to the Vice President, CMC Operations, the Head of/Senior Director CMC Operations (Drug Substance) will manage activities related to Process Development, Tech Transfer and Manufacturing of Drug substance.
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This position supports plants in the North American manufacturing network to meet the product specification, customer requirements, and shareholder expectations by improving process capability and driving process improvement projects utilizing Lean/Six Sigma methods.
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Our core service offerings include:Turnaround & Restructuring (T&R)Transaction Advisory (TA)Finance Excellence (FE)Strategic Performance Solutions (SPS)Transaction & Valuation Opinions (VAL)Retail Performance Improvement (RPI)Overview The position is in the Retail Performance Improvement practice, which provides strategic, operational and financial advisory services to high-performing growth-oriented retail and/or consumer product companies.
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Experience with lipid nanoparticle formulation and purification processes, antibody conjugation chemistry, or experience with process development, engineering and manufacturing of biologic drug product processes are highly desired.
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MSP has a secondary focus on pharmaceutical inhalation test products and is the industry leader in providing the core measurement for DPI/MDI characterization applications. MSP, a Division of TSI, provides technology solutions that improve thin film deposition processes used in semiconductor manufacturing and industrial coatings applications.
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This candidate will also be leading the effort to reduce waste via process implementation and improvements, training programs, documentation and manufacturing planning following the WCM methodology.
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process improvement pharmaceutical manufacturing jobs Title: process improvement leader
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