- BlueVoyant (MD)
- Market Development Representative ( MDR ) Location: Remote in the United States Job Description: We are seeking a dynamic and detail-oriented Market ... Development Representative ( MDR ) to join our team. This individual contributor role will work collaboratively with our demand generation marketing team, operations team, and with our sales representatives to optimize the lead conversion processes… more
- Spindrift (Philadelphia, PA)
- …a critical role as we continue to grow our newest product across the US. The Market Development Representative ( MDR ) should be based in Philadelphia and ... will build the brand through direct account selling, distributor relationships, and in- market distribution, display and sampling execution. The MDR will maximize… more
- Catholic Health Initiatives (Bryan, TX)
- …primary care, Express Clinics, and imaging and diagnostic services. **Responsibilities** The Market Development Representative ( MDR ) will develop, ... Market services and service lines growth goals. The MDR will become acutely knowledgeable in specified service lines...and within guidelines set by the Executive Director of Market Development _(EDMD)_ . Coordinates internal sales… more
- Whirlpool Corporation (Lansing, MI)
- …in the Territory Sales Representative (TSR) role and ready to advance to the Market Development Representative ( MDR ) rotation + Drive in-store rate ... for coaching and developing 6-8 direct-reports who are in their Territory Sales Representative rotation of the Real Whirled Leadership Development Program. The… more
- Medtronic (Northridge, CA)
- …that monitors Medtronic's surveillance program including the intake, protocol development , evaluation, processing, and follow-up on adverse reports, participation in ... + Assess project issues and supports project team in development of resolutions to meet goals and objectives +...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Mounds View, MN)
- …+ Familiarity with these regulations: FDA 21 CFR Part 820, EU 217/745 (EU MDR ) + Familiarity with these standards: ISO 13485, ISO 14971, IEC 60601. + Experience ... medical devices. + Experience in Systems Engineering or product development . + Advanced degree in Systems Engineering. + Experience...within the Responsibilities section of this job description are representative of those that must be met by an… more
- LSI Solutions (Victor, NY)
- …employees dedicated to advancing minimally invasive surgical instruments through research, development , manufacturing, and marketing. We have doubled in size in just ... device regulations and standards to the company throughout the development cycle. Regulatory Associates monitor regulations, standards, policies, and guidance… more
- BD (Becton, Dickinson and Company) (Warwick, RI)
- …internal audits, Notified Body assessments, FDA audits, adverse event reporting, post- market surveillance, and quality systems compliance. This position is key in ... internal audits, Notified Body assessments, FDA audits, adverse event reporting, post- market surveillance, and quality systems compliance. This position is key in… more
- Medtronic (Minneapolis, MN)
- …partners on compliance gaps, data, and/or resulting corrective actions. * Own development of training and awareness programs for SaMD, SiMD, and product security ... security enhancement. * Possess understanding of Software Bill of Material (SBOM) development and maintenance for the purposes of vulnerability monitoring. * Possess… more
- Globus Medical, Inc. (Methuen, MA)
- …technology division is searching for an enthusiastic Senior Director of Product Development to lead our navigation and computer vision team. This leadership position ... navigation program within Globus Medical and set the standard for product development , research and innovation within the industry. The position will be hands-on… more
- Medtronic (Carlsbad, CA)
- …plc, we focus on providing Engineering support for Design and Development , Quality Compliance, and Risk Management activities across the Ventilation Service ... are conducted in compliance with the FDA Quality System Regulations and EU MDR requirements. This position will focus on software design changes. * Responsible for… more
- Danaher Corporation (Richmond, IL)
- …registration maintenance, device listing, regulatory requirements, Importer and Authorized Representative actions. + Experience with ISO 13485:2016, IVD/ MDR ... to bring IVD (In-Vitro Diagnostic), Research (RUO) and Laboratorial products to market and support activities related to Quality Management System (QMS) to ensure… more
- AbbVie (North Chicago, IL)
- …serves as Deputy Person Responsible for Regulatory Compliance under EU MDR 2017/745, providing compliance subject matter expertise to internal business partners, ... Serves as the Deputy Person Responsible for Regulatory Compliance under EU MDR 2017/745, supporting quality management supervision under the direction of the… more
- Medtronic (San Diego, CA)
- …you will be asked to manage and guide the design quality engineers in the pre- market design and sustaining space. You will be responsible to drive development of ... implements all quality aspects of the company's design and development of new and sustaining medical device products** or...to ensure project planning is complete end-to-end, for both pre- market and post- market activities. + Manages activities… more
- Medtronic (Los Angeles, CA)
- …members from Systems Engineering, R&D/ Design, Manufacturing Operations, Pre & Post Market Quality, and Regulatory Affairs to ensure the successful execution of ... function as the subject matter expert that leads risk management development activities & generating tailored risk documentation outputs across different components… more
- LSI Solutions (Victor, NY)
- …to obtain market approvals in the USA (510(k), Canada, Europe (MDD/ MDR ), Australia, and ROW ensuring all US/EU/CA requirements and corporate policies and ... and Regulatory compliance with all standards that govern the design, development , manufacturing, and distribution of our medical devices. REPORTS TO: REGULATORY… more
- Actalent (Emerson, NJ)
- …and international markets. Responsibilities + Serve as the appointed Management Representative . + Lead, coordinate, author, and review regulatory filing documents. + ... files, including 510(k) submissions, Device Master files, technical files, and post- market surveillance for product changes and new products. + Collect documentation… more
- Globus Medical, Inc. (Methuen, MA)
- …Medical + Lead, manage and develop a small multi-disciplined product development team including electrical, mechanical, software, and systems engineering + ... efforts and complaints to maintain product performance and quality in the market + Lead the project portfolio including driving discipline to Globus Medical's… more
- Philips (Bothell, WA)
- …team to improve quality and compliance outcomes. + Act as the management representative for all key regulatory agencies for product safety and quality (eg: US ... FDA, EU MDR , TGA, MHLW, NMPA, etc.). Develop and maintain an...members. Acts as a coach and co-own the career development plans of your team members. **You're the right… more