• Dexian - DISYS (Golden Valley, MN)
    medical applications, and generally accepted therapy.Basic human anatomy, physiology, and medical knowledge.Basic knowledge of medical device industry and ... department process.Maintain awareness of regulations including, but not limited to: device tracking, complaint handling, and quality systems.Maintain knowledge… more
    JobGet (05/28/24)
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  • Arthrex (Pendleton, SC)
    …as FMEA, FTA, FMECA) tools are highly desirable. Experience in working in Medical Device industry, CAPA, Complaint Management, and Nonconformance Reporting ... Arthrex, Inc. is a global medical device company and a leader...in orthopedics. Arthrex is actively searching for a QA Specialist II - Sterilization to maintain Arthrex Manufacturing Inc… more
    JobGet (05/28/24)
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  • Rose International (Newton, MA)
    …Engineering, Quality Assurance, SAP Nice To Have Skills/Attributes: Agile, CAPA, Medical device , Quality Engineer Job Description **Only those lawfully ... * No travel required. Preferred Knowledge/Skills, Education, and Experience * Prior Medical Device /Biotech experience * Prior experience with a Document Control… more
    JobGet (05/28/24)
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  • Complaint Specialist

    Kelly Services (Horsham, PA)
    Kelly Services is actively seeking a Complaint Specialist - Medical Device for a long term (1+ year) hybrid engagement with one of our global clients ... including Quality Assurance and/or Quality Control in a high-volume complaint handling unit with medical device...in a high-volume complaint handling unit with medical device or combination product reporting responsibilities… more
    Kelly Services (05/09/24)
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  • Associate Director - Device Safety…

    Lilly (Indianapolis, IN)
    …support communities through philanthropy and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage ... clinical and scientific expertise working across Lilly's device product portfolio to lead the completion of safety...the EU Qualified Person and EU Authorized Representative for medical devices **Minimum Qualification Requirements:** + Any of the… more
    Lilly (05/19/24)
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  • Complaints Specialist I

    Terumo Medical Corporation (Elkton, MD)
    …(KSA)** + Requires a minimum 2 years experience in a quality or customer service/ complaint resolution in medical device industry (disposable devices). + ... of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $5+ billion in...and Terumo Medical Products. **Job Summary** The Complaint Handling Specialist I is responsible for… more
    Terumo Medical Corporation (04/30/24)
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  • Product Surveillance Specialist

    Bausch + Lomb (Kirkwood, MO)
    …of communication between manufacturer, distributors and competent authorities for all medical device complaint related activities, including assistance ... + Provide understanding, leading analysis and management of information regarding medical device complaint events and/or adverse events,… more
    Bausch + Lomb (03/27/24)
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  • Product Surveillance Specialist

    Bausch + Lomb (Clearwater, FL)
    …of communication between manufacturer, distributors and competent authorities for all medical device complaint related activities, including assistance ... + Provide understanding, leading analysis and management of information regarding medical device complaint events and/or adverse events,… more
    Bausch + Lomb (04/25/24)
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  • Post Market Surveillance Specialist

    Actalent (Minneapolis, MN)
    …the Implant Registry database Skills: Complaint analysis, biomedical engineering, complaint handling, medical device , Quality Top Skills Details: ... Complaint analysis,biomedical engineering, complaint handling, medical device Additional Skills & Qualifications: Bachelor's Degree in STEM Required… more
    Actalent (05/16/24)
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  • QA Specialist I (Combination Product)

    US Tech Solutions (Austin, TX)
    US- Medical Device group Location: Local to Austin, TX M-F 8-4:30/5 Hybrid, 3 days in office, 2 remote following training + Individual will work in global quality ... organization processing pharmaceutical, ** medical device and combination product complaints and... complaint documentation,** investigation, and review of all **non- medical complaint content.** Responsible for reviewing … more
    US Tech Solutions (05/29/24)
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  • Post Market Surveillance Specialist

    Actalent (Minneapolis, MN)
    …the Implant Registry database Skills: Complaint analysis, biomedical engineering, complaint handling, medical device , Quality Additional Skills & ... from written, electronic, and oral communications are entered the complaint handling database in accordance with procedure. + Contacts...Bachelor's Degree in STEM Required + Experience in a medical device manufacturing or quality role is… more
    Actalent (05/16/24)
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  • Postmarket Surveillance Specialist II

    BioFire Diagnostics, LLC. (Salt Lake City, UT)
    …+ Analytical Skills + Time Management + Ability to work independently + Ability to follow detailed processes + Knowledge of medical device regulation preferred ... are expected. As guided by work instruction documents, the PSS will review the complaint investigations for medical d evice reporting and work with senior … more
    BioFire Diagnostics, LLC. (05/08/24)
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  • QA Specialist I

    Kelly Services (Austin, TX)
    …will work in our client's global quality organization processing pharmaceutical, medical device and combination product complaints and inquiries. Interface ... requirements. *Product complaint documentation, investigation, and review of all non- medical complaint content. Responsible for reviewing medical more
    Kelly Services (05/13/24)
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  • Intake Specialist I

    Kelly Services (Austin, TX)
    …at your convenience. Thank you for your time and consideration. TITLE: Intake Specialist I PAY: $20-21/hr (DOE) DURATION: 6 months LOCATION: On-Site - Austin, TX ... require both remote and in-person availability. **Purpose:** The Intake Specialist I works to support PMQA through providing the...the customer to make the initial identification of the complaint code. They will conduct data entry and coordination… more
    Kelly Services (05/14/24)
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  • Quality Specialist III

    ThermoFisher Scientific (West Hills, CA)
    …of ISO 13485 and GMP regulations which govern a medical device and diagnostics manufacturing. Knowledge of complaint handling requirements. + Trending ... **Job Description** **Position Summary:** Quality Specialist III, Post Market Surveillance (PMS) and Stability...data analysis, reporting, trending, and documentation review, coordination of complaint and lot qualification data, device history… more
    ThermoFisher Scientific (05/22/24)
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  • Field Clinical Specialist , Indianapolis,…

    Edwards Lifesciences (Indianapolis, IN)
    …cardiac surgery or interventional cardiology are strongly preferred; candidates with other relevant medical device clinical sales support experience will be + A ... the world. As a part of the Field Clinical Specialist team, you will be a critical part of...Specialists will provide guidance on the use of the device , thereby enabling physicians and staff to reach expert… more
    Edwards Lifesciences (05/26/24)
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  • Quality Systems Specialist III

    Agiliti Health (Eden Prairie, MN)
    …of applicable experience + Experience with ISO 13485, 21 CFR Part 820, and Medical Device Good Documentation Practices + Familiarity with managing 21 CFR Part ... **Job Description:** The Quality Systems Specialist roles are responsible for providing support for...806, Medical Device ; Reports of Corrections and Removals… more
    Agiliti Health (05/21/24)
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  • Quality Compliance Specialist (Complaints)

    Regeneron Pharmaceuticals (Troy, NY)
    …This role may be for you if you: + Are experienced in pharmaceutical or medical device complaint investigation + Have an understanding of biologics ... We are currently looking to fill a Quality Compliance Specialist (Complaints) position. This position maintains site compliance of operations focused primarily on… more
    Regeneron Pharmaceuticals (05/17/24)
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  • Quality Specialist 2 - Product…

    GE HealthCare (Wauwatosa, WI)
    …Excellent interpersonal, organizational, and influencing skills. + Familiarity with the application of medical device as it relates to patient safety. + Ability ... **Job Description Summary** Manages complaint handling activities and supports key Quality &...in broad area. GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is… more
    GE HealthCare (05/14/24)
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  • Security Specialist I

    Service Source (St. Louis, MO)
    …who drive innovation, embrace change, and serve humanity. Job Summary The Security Specialist I is an entry level position made up of three components: Visitor ... policy. + Open and close alarmed facility using Arming Device and Combination Lock. + Check security badges to...complete the application process please contact the Program Outreach Specialist in your region using the list below. Step… more
    Service Source (04/17/24)
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