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Advanced degree (BS, MS or PhD) in Chemical/Biochemical Engineering, Biochemistry, Immunology, or related degree with experience (8+ for BS, 5+ for MS, 2+ for PhD) in process development and manufacturing sciences in cell therapy, biotechnology, or pharmaceutical industry.
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Possess continuous improvement experience with emphasis in the laboratory information management and deployment of LEAN/Six Sigma, analytical methods and manufacturing process development for polymeric materials.
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As we continue to grow, we are seeking a skilled and motivated Process Engineering Manager to lead our manufacturing processes in Woburn, Massachusetts. Strong knowledge of heat exchanger and cold plate manufacturing processes.
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Lead an Attribute Sciences team to support synthetic small molecule, synthetic peptide, and/or SiRNA drug substance and drug product process development, manufacturing, release & stability testing and characterization.
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Senior Systems Engineers for Randstad Digital, LLC. Multiple openings. Use WebSphere, JBoss, IBM HTTP Server, SOLR, WXS, Java, J2EE, WAS, Tomcat, Apache, Unix, Shell, Wrapper, Ansible, Python, Horizon, BitBucket, Git, Artifactory, Celestial, Docker, Splunk, Container, Jenkins, CI/CD, XL, JDBC, Tivoli Performance Viewer, Wily, Log Analyzer, Thread Analyzer, Heap Analyzer, Introscope, Dynatrace, AppDynamics, TrueSight, MQ. 40 hrs/wk.
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Proven laboratory expertise in radioactive product development or manufacturing, radiochemistry, including radiochemical separations and chemical synthesis. QSA Global, Inc. specializes in supplying state of the art gamma radiography and portable X-ray systems used in non-destructive testing (NDT) as well as high-performance radiation sources used in oil well logging (OWL), industrial processes, and nuclear medicine.
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Work closely with colleagues in Process development to design and implement new technologies for aseptic filling of cell therapy drug products in novel device platforms; this includes working closely with Contract Development and Manufacturing Organizations (CDMOs) and engineering firms to design processes and equipment needed to perform aseptic filling operations in a GMP environment.
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The Director of Drug Substance Manufacturing at QurAlis plays a pivotal role in developing and optimizing chemical processes for Oligonucleotides production and overseeing the refinement of external manufacturing processes.
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Must have strong knowledge of biologics and small molecules manufacturing, materials management, quality control, quality assurance and CMC regulatory requirements. Responsible for all aspects drug substance including conjugation process development, validation, characterization, scale-up, tech transfer, analytical method qualification, specifications, release and stability testing.
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Job titles: CEO, CFO, COO, CPO, Vice President of Finance (VP Finance), Vice President of Operations (VP Operations), Vice President of Purchasing (VP Purchasing), Vice President of Procurement (VP Procurement), Senior Vice President of Finance (SVP Finance), Senior Vice President of Operations (SVP Operations), Senior Vice President of Purchasing (SVP Purchasing), Senior Vice President of Procurement (SVP Procurement), Executive Vice President (EVP.
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Education : Undergraduate degree required in either of the following engineering disciplines: Electrical Engineering (EE), [Electrical]Computer Engineering (ECE), Mechanical Engineering, Robotics, Biomedical Engineering, Chemical Engineering, or Industrial Engineering.
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Graduate of an X-ray technician program accredited by the Joint Review Committee on Education in Radiologic Technology (JRCERT) or another accrediting agency approved by The American Registry of Radiologic Technologists (ARRT.
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In addition, the Cash Application Specialist will be responsible for supporting the collections team posting customer receipts, payments, remittances, and credits as necessary and processing of payments received through the Lockbox, Credit Cards and ACH processes.
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Process Optimization: Identify opportunities to enhance manufacturing processes for optical components and systems, focusing on efficiency, quality, and cost-effectiveness. · Continuous Improvement: Lead initiatives to identify and implement process improvements, leveraging tools such as lean manufacturing, Six Sigma, and statistical process control (SPC) methodologies.
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Maintain data integrity in compliance with GCP, relevant SOPs and regulatory requirements by reviewing data processes and filing documentation in the trial master file (TMF) Comprehensive understanding of database and dictionary structures (e.g., MedDRA, WHO DRUG.
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another name process synonyms chemical manufacturing term titles words dictionary engineers word processes jobs in Woburn, MA
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