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Support employees by troubleshooting tickets, email and phone requests. Install, troubleshoot, and repair audio visual equipment used in meeting rooms. Act as collaboration tool admin (Teams, Webex, Zoom) in requests, training, and support. Develops knowledge base articles for end user reference. Performs routine and non routine preventative maintenance in accordance with
Posted 21 days ago
s. The Individual Bachelor's degree in a scientific or related discipline; or equivalent combination of education and experience. RAC (Regulatory Affairs Certification) is a plus. 10 years+ of experience in a regulated Medical Device Industry required; In Vitro Diagnostic or Biologics Industry experience preferred. 7+ years of experience developing and executing regulatory
Posted 14 days ago
Trains employees. Colorado State Posting Details This position's starting salary is between $89,500 and $161,000 per year, and it is bonus eligible. Salary will be determined by education, experience, knowledge, skills, and abilities of the candidate, in addition to internal equity and alignment with market data. Ortho offers a comprehensive benefits package, including me
Posted 22 days ago
Interfaces with Clinical Labs Strategic Business Unit and R&D during new product development, ensuring Ortho Care launch readiness for new product introductions. Global Ortho Care interface to other functions to support company initiatives and lifecycle management projects, ensuring that Ortho's portfolio is profitable and supportable. Proactively monitors global customer
Posted 14 days ago
Team leader for targeted solutions sales and assigned client Process Excellence assessments and engagements. Develop solutions with a primary focus on LEAN, in potential customer facilities (healthcare institutions). These Process Excellence engagements are driven from VAS automation and Transfusion Medicine product sales opportunities. Own and be accountable for the Valu
Posted 22 days ago
Contributes to refinement, translation, allocation to subsystems, and management of stakeholder requirements. Contributes to definition of system interfaces, evaluates systems and makes solution recommendations. Contributes to cross discipline feasibility and tradeoff studies. Contributes to subsystem level design and technical reviews. Contributes to defect management, r
Posted 14 days ago
Manage the calibration workload through the use of ProCal V software. Execute all calibrations to meet daily, weekly, annual production. Maintain records through proper documentation in the ProCal V system of record. Identify any issues and address them through in a cGMP compliant manner. Maintain an open line of communication with customer base. Participates and collabor
Posted 23 days ago
Conducts prototype assembly, testing, and analysis within a larger R&D activity. Develop, assemble, and test products to support existing project programs. Design, build, and utilize engineering test fixtures for subsystem evaluation. Fabricate prototype subsystem/fixture parts in on site machine shop. Oversee maintenance, safety, and training protocols for on site machin
Posted 14 days ago
Develop strategy for end to end, global multi channel marketing campaigns for product and service offerings Provide subject matter expertise and guidance to cross functional and supporting teams to ensure quality development and seamless execution of campaign tactics and sales collateral. Build, and provide oversight of marketing processes for campaign briefs, branding, m
Posted 23 days ago
Development and validation of biomaterials to support MicroWell immunoassays. Conjugation and purification of biomaterials to be used in MicroWell immunoassays. Analytical characterization of antibodies, antigens, and other biomaterials. Supports laboratory procedures creating novel materials and formulations intended for use in the development of new in vitro diagnostic
Posted 14 days ago
Authors, reviews and/or approves validation documentation including protocols, reports and other sources of information to ensure that validations and procedures are consistent with current industry standards and regulatory requirements. Ensures that validation and qualification activities are consistent with company validation policies and procedures. Proceeds according
Posted 24 days ago
Effectively communicates verbally and in writing. Demonstrates a sense of urgency to complete production schedule on time. Accepts personal responsibility for the quality and timeliness of work. Accurately and timely completes all required reporting functions using an SAP/ERP computer system. Uses computer based documentation system to find, view and print specifications
Posted 15 days ago
Manage delivery of MDM engagement using Agile or Waterfall methodologies Develop highly performant, reliable, and scalable MDM and Data Governance solutions for Customer, Product etc. Coach and develop team members to overcome technological challenges Communicate with business, IT and other entities to understand data ecosystem, business requirements and be able to transl
Posted 24 days ago
Oversees all day to day production planning and purchasing to ensure production schedules and other business deliverables are met. Escalates and coordinates resolution of material shortages as needed. Manages S&OP Supply Planning Process Analyzes demand signals and generates a consensus production plan for inclusion in WW S&OP roll up. Collaborates with key business partn
Posted 15 days ago
Provides subject matter expertise for IVD clinical strategy, clinical trial design, and operations to ensure studies and programs are delivered on time, within budget, and with a high quality outcome. Drives performance and delivers outcomes with external stakeholders (staffing agencies, regulatory authorities, etc.) Creates and maintains key clinical trial documents such
Posted 27 days ago
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