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Maintains proper documentation through the Computerized Maintenance Management System (CMMS). Complies with company safety, quality, standard operating procedures (SOP) and HACCP guidelines.
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This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, relevant regulations (e.g., 21 CFR Parts 312 and 314, EMA Clinical Trials Directives), and Standard Operating Procedures (SOPs) as appropriate.
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Element has an upcoming opportunity for a Laboratory Analyst (PFAS) to join our growing team in Fort Wayne, IN. The Laboratory Analyst (PFAS) prepares and analyzes Environmental samples using standard analytical techniques according to approved scientific and EPA methodology in compliance with Element Materials Technology Testing Quality Assurance programs and standard operating procedures (SOPs.
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Redline and/or create Standard Operating Procedures and FMEA to support manufacturing. Nexus Pharmaceuticals is hiring for a Manufacturing Documentation Specialist. Manufacturing Documentation Specialist.
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The Industrial Solutions CAD Designer will support the Engineered Systems (ENSY) team and the sales team by developing and delivering system layout drawings and other engineering documentation to support ENSY projects and standard product offerings.
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Complete all required documentation and adhere to all SOP/WKI procedures that apply to running or changing over packaging equipment. Ensure assigned packaging resources are changed over and operating at the production standard while meeting all safety and quality expectations.
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Create or revise laboratory Standard Operating Procedures or other applicable laboratory focused documentation to support QC and PD during commissioning and startup. Create or revise laboratory Standard Operating Procedures or other applicable laboratory focused documentation to support QC and PD during commissioning and startup.
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Provide training support services including development of CANES system training requirements and documentation of those requirements in the CANES Navy Training System Plan (NTSP). Develops Navy Standard courses implementing the training solutions and conducts CANES technical training.
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Must be capable of operating a standard 1/2-ton pick-up for occasional delivery and pick-up of materials and personnel and hold a valid, unrestricted motor vehicle operator's license issued by the state of residence, and the manual dexterity necessary to operate a standard desktop computer keyboard.
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90%) Bench level electronic and electro-mechanical repair tasks using industry standard trouble shooting, repair and soldering skills. (10%) Documentation of actions taken on each item and communication of completions, obstacles and concerns.
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Reception, processing, combining and transmission of standard analog and digital CATV services, high speed and telephony duties as directed by Supervisor. Ability to perform regular proof of performance and other headend and plant testing, documentation and reporting in accordance with FCC rules.
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Document process steps on appropriate batch documentation. Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product. Document process steps on appropriate batch documentation.
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Clinical Documentation Specialist. The Clinical Document Specialist will provide support to the TMF content owners on one or more clinical programs. This position will work closely with the Study Management Teams (SMT) to ensure that the TMF is kept both current and inspection ready according to SOPs and applicable regulations.
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Position Summary:The Quality Control Coordinator is responsible for ensuring the adherence to established standard operating procedures by inspecting frames produced in an aluminum or metal products manufacturing environment.
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Demonstrated experience or knowledge with sponsor or CRO clinical research process, including collection of documents at study start-up, during study conduct and close-out. Experience with electronic trial master file system(s) including uploading, reviewing, quality checks (QC), approval of study required.
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