Research Salary at Us Bancorp BETA

PRIMARY OBJECTIVE: Entry level researcher position at Thomson Reuters Court Express. This person is responsible for learning CXP systems and processes, completing CXP training and working both with and without supervision on research requests. This individual will complete research requests and perform all duties as described in the CXP researcher metrics. EXPERIENCE: This is an entry level position. 6 months Legal experience preferred but not required. Bachelor's Degree preferred. KNOWLEDGE: Knowledge of court system and legal documents useful, but not required. MAJOR AREAS OF ACCOUNTABILITY: Complete CXP training program- become familiar with the US Court System and main pleadings in all types of court cases. Become competent with all DRR/DD research tools, court websites, Extranet, WL, PACER, etc.- know how and when to use these search tools. Complete client requests for the appropriate department. Adhere to DRR/DD performance metrics. Provide professional, informed answers to clien

R&D Engineer 6-month contract to hire Note: We do not hire C2C Author and execute Process Validations including Test Method Validation (TMV), Inspection Method Validation (IMV), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Product Performance Qualification (PPQ) Responsible for process development, equipment specification, acquisition and implementation. Understands engineering principles theories, concepts, practices and techniques. • Analyzes and solves problems from basic engineering principles. • Completes design of experiments, validation, completion of testing and analysis of data for continuous improvement activities. Presents data to equipment teams. Suggests and supports new methods or materials for continual improvement of quality and efficiency. Analyzes current equipment for process suitability and provides detailed plans for improvement Creates and revises manufacturing documents, specifications, standard operating proced

Duration: 12 Months Contract (Possible Extension) Onsite Job Purpose Develops products, materials, processes, or equipment for projects of moderate complexity. Under limited supervision/guidance, compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials. Key Responsibilities Fully participates in and successfully contributes to project teams typically including the following activities: product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process/test documentation. Works independently to plan and schedule own activities necessary to meet timelines. Designs and coordinates standard engineering tests and experiments. Designs, procures, and fabricates tooling and fixtures. Performs troubleshooting on new products/process problems as related to

Key Responsibilities: Support design changes and conduct design change analysis for materials and components impacted by obsolescence. Ensure standards compliance (e.g., FDA, ISO) for material changes and documentation. Collaborate with cross-functional teams, including R&D, Quality, Regulatory, and Operations. Participate in and approve change notices; coordinate with vendors to collect and analyze technical data. Prepare DV (Design Verification) reports, protocols, and support submission documentation for regulatory changes. Manage documentation, including drawings, labeling updates, packaging changes, and part replacements. Potential hands-on work in the lab, but majority of the work is focused on documentation, compliance, and analysis. Preferred Experience & Skills: 5+ years of engineering experience in the medical device industry. Strong sustaining engineering background with hands-on experience in design and product lifecycle management. Experience with catheter devices – corona

A medical device company is looking to hire a Clinical Research Specialist, onsite in Maple Grove, Minnesota. This direct hire employee will report to the Director of Clinical Operations and under their general supervision, will develop, coordinate, administer the logistical aspects of clinical trials according to GCP and SOPs. This person will act as a pivotal point of contact and communication between department staff, clinical sites, as well as vendors. What You'll Do: Develops, tests, and implements clinical tools to provide relevant information for clinical studies management. Manages clinical study site information and documentation. Requests, tracks, reviews and assures receipt of proper study documentation (IRB approval letters, Signature Pages, Informed Consent materials, signed Clinical Study Agreements, Confidentiality Agreements, etc.). Obtains, reviews, and files site personnel documentation to ensure site compliance. Develops and distributes clinical study documents (Prot

**By joining Bio-Techne, youll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** **Position Summary:** As a Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. **Key Responsibilities:** + Prepare conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research according to written SOPs. Occasionally develop new procedures for new products. + Perform in-process testing of conjugates stocks used in Bio-Techne assay platforms. + Complete post-manufacturing processing, sterile filtering, vialing, and labelling

Overview: Research Coordinator, Land Development - Minneapolis, MN Westwood Professional Services, Inc. Westwood Professional Services, Inc. is seeking a Research Coordinator for the Land Division to join our team in our Minneapolis, MN office. The Research Coordinator will play a critical role in supporting the Land Division by conducting site investigations, preparing feasibility reports, and performing zoning and planning due diligence. This position will involve collaborating with various teams to ensure compliance with permitting and platting requirements, while providing data-driven insights to facilitate informed decision-making. Duties and Responsibilities: Assist Market Leaders (MLs) and Project Managers (PMs) with various reporting tasks. Conduct comprehensive site investigations to assess land suitability for development projects. Prepare detailed feasibility reports that evaluate potential development sites, including analysis of zoning regulations, land use compatibility,

Job Description: Job Title Sr Research Engineer* Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so its equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a diversity of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. This position provides an opportunity to transition from other private, public, government or military experience to a 3M career. The Impact Youll Make in this Role The person hired for this position will join the Personal Safety Division and will be part of a team of engineers and scientists who design and develop innovative and high-quality respiratory solutions for our customers to protect people. The materials developed by this team include the next generation of filter media as well as the personal protective equ