- Fresenius Medical Center (Ogden, UT)
- …control activities. + Support Product Center/Project Manager to get part needed to Medical Device Compliance and Regulatory Affairs to complete Technical ... development and design changes and take accountability for quality compliance as a member of the cross-functional project team...+ Autonomy in decision making. + Advanced knowledge of medical device regulations (NMPA regulation, MDD 93/42/EEC,… more
- Compass Group, North America (New York, NY)
- …Technology Solutions, and Ambulatory EVS. Learn more at www.Crothall.com. Job Summary The Medical Device Integration and Cybersecurity specialist will be ... Utilizing Crothall's cybersecurity framework, technologies and policies and procedures, the Medical Device Integration and Cybersecurity Specialist will… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Senior Specialist Medical Device and Combination Product (MDCP) engineer is a key technical leader of regulatory and ... groups, Regulatory Affairs, Procurement and suppliers. Knowledge of design control, medical device , combination products, drug delivery, pharmaceuticals and… more
- ICU Medical (Dublin, OH)
- The Device Sales Specialist is responsible for building and maintaining relationships with key decision makers that lead to future business opportunities. The ... other than Colorado; California; Connecticut; Montana, Maine or New York. **Title:** * Device Sales Specialist - Ohio / Western Pennsylvania* **Location:**… more
- ICU Medical (UT)
- *Position Summary* The Device Sales Specialist is responsible for building and maintaining relationships with key decision makers that lead to future business ... and will not be discriminated against on the basis of disability. **Title:** * Device Sales Specialist - Pacific Northwest* **Location:** *United States - Remote… more
- ThermoFisher Scientific (Middletown, VA)
- …Middletown, VA Specialty Diagnostics Group (SDG) **How will you make an impact?** The Medical Device Complaint Handling Specialist III is responsible for ... + Detailed knowledge of ISO 13485 and GMP regulations which govern a medical device and diagnostics manufacturing. + Strong analytical and problem-solving skills… more
- Abbott (Princeton, NJ)
- …requisition. We are building a candidate slate for a future opening**_** Product support specialist - Medical device - Abbott Point of Care (APOC) /Associate ... of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...Technical Support Specialist **Working at Abbott** At Abbott, you can do… more
- Abbott (Maple Grove, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...Maple Grove, MN currently has an opportunity for a ** Device Accountability Specialist ** . This new team… more
- Rep-Lite (Los Angeles, CA)
- …operating room and / or urology: this opportunity is tailored for you. Apply now! Clinical Specialist - Urological Medical Device Sales About Us: We are a ... leading innovator in urological medical devices, dedicated to enhancing the well-being of men...team as Clinical Specialists. Key Responsibilities: As a Clinical Specialist , you will play a pivotal role in driving… more
- Lilly (Indianapolis, IN)
- …support communities through philanthropy and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage ... + Review device surveillance processes, procedures, and/or report templates to ensure compliance with global device regulations. + Serve as a contact person… more
- Edwards Lifesciences (Irvine, CA)
- …also ensure compliance with regulations and manage the lifecycle of device inventory and accountability to support clinical trials. _The position will be on-site ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
- California Energy Commission (Sacramento, CA)
- Compliance Analysis Program Specialist ELECTRIC GENERATION SYSTEM PROGRAM SPECIALIST I $9,639.00 - $12,059.00 per Month Final Filing Date: 5/7/2024 Job ... Details Job Code #: JC-428624 Position #(s): ###-950 Working Title: Compliance Analysis Program Specialist Classification: ELECTRIC GENERATION SYSTEM PROGRAM… more
- Amazon (Bellevue, WA)
- …TV and Echo Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to ... Notified Bodies. About the team The Quality & Lean, Medical Devices Operational Compliance Center (MD-OCC), consists...verbal, presentation, and organizational skills. - . Experience with medical device software requirements. - . Ability… more
- HonorHealth (Scottsdale, AZ)
- …to learn more. HonorHealth is looking for an RN Ventricular Assist Device (VAD) Clinical Manager to support our new, inviting and exciting Program. ... area. The comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer… more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill a Quality Compliance Specialist (Complaints) position. This position maintains site compliance of operations focused ... hypothesis and writes technical reports to support investigation conclusions. Compliance Operations are inclusive of, but not limited to,...you if you: + Are experienced in pharmaceutical or medical device complaint investigation + Have an… more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill a Quality Compliance Specialist (Complaints) position. This position maintains site compliance of operations focused ... you if you:** + Are experienced in pharmaceutical or medical device complaint investigation + Have an...minimum amount of experience for each level: + Quality Compliance Specialist : 2+ years + Sr. Quality… more
- Stryker (Mahwah, NJ)
- …MDR/MDV reporting and product recalls + In-depth knowledge of FDA and international medical device regulations and standards (CFR, MDD, QSR, ISO 13485, CMDCAS, ... information is available at www.stryker.com We are currently seeking a **Senior Specialist , Regulatory Compliance ** to join our Joint Replacement Division based… more
- Mentor Technical Group (Juncos, PR)
- …knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... System which provides a framework for measuring and improving our performance. Compliance Specialist 2018 2 Job Description GIDEP). + Act as a point of… more
- ICU Medical (Lake Forest, IL)
- …US state or territory in good standing . Minimum 7 years experience in medical device industry . Minimum 5 years of clinical experience *Minimum Qualifications* ... discriminated against on the basis of disability. **Title:** *Senior Clinical Specialist , Medical Affairs (Hybrid)* **Location:** *IL-Lake Forest* **Requisition… more
- Abbott (Alameda, CA)
- …*Perform other related duties and assignments as required. *Accountable for meeting the compliance requirements for Medical Device Reporting (803), including ... in observations from regulatory agencies. **Accountability/Scope/Budget** Accountable for meeting the compliance requirements for Medical Device Reporting… more