- BioAgilytix (Boston, MA)
- …manages system Standard Operating Procedures (SOPs), as neededCreates and manages validation documents in internal quality management systemsResponsible for ... therapeutics to the patients who need them.In this role, you will perform validation studies through the analysis of biological samples. Our clients trust us to… more
- CIRCOR International, Inc (Corona, CA)
- …STRUCTUREBUSINESS: Aerospace & DefenseLOCATION: CoronaDIRECT REPORTING: Sourcing & Supply Quality ManagerAbout CIRCOR Aerospace & Defense CIRCOR Aerospace & Defense ... with experience working in a manufacturing environment. The Sourcing Specialist will be an integral part of Supply Chain...Supply Chain Team and will work closely with Supplier Quality , Buyers and Sourcing Specialists to execute a time-sensitive… more
- DivIHN Integration Inc (Round Lake, IL)
- …shall work towards developing/sustaining a product in accordance with Client's defined Quality and Regulatory standards. 9. The Principal RandD Engineer shall ... inquiries regarding the following opportunity, please contact one of our Talent Specialist Sivanesan | 2243690756 Title: Lead RandD Engineer Location: Round Lake, IL… more
- Medtronic (Northridge, CA)
- …90,000+ employees in more than 160 countries. **A Day in the Life** As Principal Regulatory Affairs Specialist , you will develop and implement medical device ... from regulatory agencies. + As an individual contributor, the Principal Regulatory Affairs Specialist is responsible for...AI, Cybersecurity, IEC 62304/82304_** **)** + Software Development & Validation for class B & class C + Risks… more
- Sierra Nevada Corporation (Austin, TX)
- …to ensure compliance with all government requirements and internal procedures. As a Principal EVM Specialist , you will develop internal processes and procedures, ... in depth earned value data analysis, inclusive of data quality checks and CDRL/SDRL (IPMDAR, CFSR, CSDR, etc.) review....relevant stakeholder learning sessions + Experience in Earned Value validation or re- validation + Experience in successful… more
- Portland General Electric (Tualatin, OR)
- …and accessible to all. _This position is posted at 2 levels, Senior and Principal . There is only 1 position available to fill. Level will be determined during ... the interview process._ **Senior Technical & Data Analyst or Principal Technical & Data Analyst** **Job Function: Technical and Data Analytics** Manages … more
- Northrop Grumman (Baltimore, MD)
- …making history. **Northrop Grumman Mission Systems (NGMS)** is seeking a dedicated **Sr. Principal Quality Engineer** to join our team in **Baltimore, MD.** This ... is a **Second Shift** position. **What You'll Get to Do:** The Sr. Principal Quality Engineer develops, modifies, applies and maintains quality evaluation… more
- Paccar Winch Inc. (Louisville, KY)
- Quality Specialist Apply now " Apply now + Apply Now + Start applying with LinkedIn Start + Please wait Date: Apr 18, 2024 Location: Louisville, KY, US, 40258 ... Company: PACCAR Job Title: Quality Specialist Company Information PACCAR is a...services, information technology and truck parts related to its principal business. Whether you want to design the transportation… more
- Splunk (IL)
- …Experience team as we look to scale our digital accessibility program! As a ** Principal Accessibility Software Engineer** , your role will be crucial to growing the ... improvements, validate fixes + Provide training to empower teams to own web accessibility quality + Mentor and coach other engineers, share the work you are doing,… more
- Colgate-Palmolive (Topeka, KS)
- …reason to smile and join our global team! **Job Summary** The role of a Quality Documentation Specialist is to maintain the site document management system (DMS) ... against regulatory requirements and compliance with the Colgate Quality Standards. This role is also responsible for assisting the quality department in… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …: 0-2+ years + QA Microbiology Specialist : 2-5+ years + Sr QA Microbiology Specialist : 5+ years + Principal QA Microbiology Specialist " 8+ years Must ... The QA Microbiology department is hiring! The QA Microbiology Specialist - Drug Product assists in the planning, coordinating, and facilitating of activities… more
- University of Michigan (Ann Arbor, MI)
- Research Lab Specialist Inter Apply Now **How to Apply** A cover letter is required for consideration for this position and should be attached as the first page of ... seeking an energetic, highly motivated individual for a Research Lab Specialist Intermediate/Associate in the therapeutic oncology team. The successful candidate is… more
- University of Michigan (Ann Arbor, MI)
- …databases to organize healthcare-related data using REDCAP. + Ensure data integrity and quality by performing periodic data cleaning and validation procedures. + ... Research Area Specialist Sr/Intermediate (Data Manager) Apply Now **How to...including data transformation and standardization. + Collaborate with statisticians, principal investigators, and other researchers to understand data requirements… more
- Merck (West Point, PA)
- **Job Description** We have an exciting opportunity for a Senior Specialist position in the Device Technology group within our company's Pharmaceutical Science and ... as well as ensuring that risks are appropriately identified and mitigated. The Sr. Specialist is accountable for either sole or shared project leadership, as well as… more
- UNUM (Portland, ME)
- …demonstrating strong customer service prior to movement to exempt level benefits specialist role. ** Principal Duties and Responsibilities** + Develop skills to ... for return to work opportunities as appropriate. Develop and strengthen claim validation and return to work techniques, where applicable. + Produce objective, clear… more
- University of Miami (Hialeah, FL)
- …of patient outcomes, and complexity of patient care. Serves as key resource for CDI/Coding/ Quality . The CDI Second Level Reviewer works in collaboration with CDI & ... quality leadership, CDI specialists, coders, quality analysts,...rendered, severity of illness, risk of mortality, and clinical validation (in compliance with government and other regulations). +… more
- Abbott (Maple Grove, MN)
- …with business strategies, working principally with senior management. Acts as the principal designer for SAP Quality Management and Patient Device Tracking ... Degree (Masters' Degree preferred). + 10+ years relevant experience with SAP Quality Management processes, including 3+ years as Application Architect. + 5+ years… more
- Edwards Lifesciences (Irvine, CA)
- …technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory ... control documents including technical summaries, clinical risk assessments, design of validation protocols and reports, design and application of FMEAs (Failure… more
- DATAMAXIS (Easton, PA)
- …+ Experience designing and implementing a Data LakeHouse. + Ensure data quality and accuracy by implementing validation checks and error-handling mechanisms. ... + Experience designing and implementing BI data visualizations and interactive dashboards using Microsoft Power BI. + Familiarity with SAP and SAP data in a manufacturing setting. + Participate in the design and development of the data LakeHouse, as well as… more
- Edwards Lifesciences (Irvine, CA)
- …technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory ... development of technical summaries, clinical risk assessments, design of validation protocols and reports, design and application of FMEAs...signs in the critical care setting, we focus on helping patients regain and improve the quality of their… more
