- Whirlpool Corporation (Benton Harbor, MI)
- …Second Rotation - Sell In:** After the TSR role, participants are guided into a Market Development Representative ( MDR ) role. This position will be ... track your career trajectory in the Real Whirled Sales Development Program by interacting in a variety of professional...Whirlpool's brands, products, consumers, and how we go to market . **Your First Rotation - Sell Thru:** Participants apply… more
- Veralto (MA)
- …from all backgrounds to apply to our positions. Reporting to the Director of Market Development , the _Market Development Representative_ is responsible for ... create new sales opportunities. It also involves contributing to campaign development , understanding customer personas, and achieving pipeline and revenue targets… more
- Medtronic (Los Angeles, CA)
- …that monitors Medtronic's surveillance program including the intake, protocol development , evaluation, processing, and follow-up on adverse reports, participation in ... team and stakeholders Assess project issues and supports project team in development of resolutions to meet goals and objectives. Understand current and upcoming… more
- CADDi (Chicago, IL)
- At CADDi, we are looking for a highly motivated Senior Business Development Representative to join our growing team and play a crucial role in our future growth. ... ensuring a seamless handoff of qualified executive leads. + Market Intelligence: Stay abreast of industry trends, competitor activities,...of experience in a BDR, LDR, SDR, ADR, or MDR role within SaaS and/or manufacturing, with a demonstrable… more
- Takeda Pharmaceuticals (Lexington, MA)
- …+ Provide senior-level Quality leadership and guidance across design, development , technology transfer, commercialization, and post- market surveillance. + ... all business units, geographies, and therapeutic modalities spanning Takeda's development pipeline and lifecycle management of marketed products. Drive...FDA 21 CFR Part 820, ISO 13485, ISO 14971, MDR /IVDR, MDSAP). + Act as or designate the Device… more
- Dentsply Sirona (Johnson City, TN)
- …to: **Develop faster** - with our commitment to the best professional development . **Perform better** - as part of a high-performance, empowering culture. **Shape ... an industry** - with a market leader that continues to drive innovation. **Make a...role where you will serve as the Site's Management Representative and the Person Responsible for Regulatory Compliance (PRRC)… more
- Medtronic (Mounds View, MN)
- …Reports for regulatory agency submissions and updates with experience in MDD and MDR requirements with upkeep in post- market clinical surveillance and follow-up. ... and overseeing execution of key clinical programs to support the development and advancement of best-in-class transcatheter mitral therapies. The Principal CRS… more
- Abbott (Alameda, CA)
- …Asia. Overseeing all aspects of quality and regulatory affairs, from design and development to post- market surveillance, this role ensures Lingo meets the ... your true self, and live a full life. You'll also have access to: + Career development with an international company where you can grow the career you dream of +… 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 (Irvine, CA)
- …for Regulatory Compliance for assigned Device Legal Manufacturer under EU MDR 2017/745, providing compliance subject matter expertise to internal business partners, ... for Regulatory Compliance for assigned Device Legal Manufacturer under EU MDR 2017/745, supporting quality management supervision under the direction of the… more
- J&J Family of Companies (Irvine, CA)
- …to drive support of the clinical and regulatory strategy; . May serve as the clinical representative on a New Product Development team; . May assist with the ... development of Post- Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation Reports...(ie, CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR , MEDDEV, ). . Clinical/medical background is a plus.… more
- Medtronic (Minneapolis, MN)
- …partners on compliance gaps, data, and/or resulting corrective actions. + Own development of training and awareness programs for Software as a Medical Device ... security enhancement. + Possess understanding of Software Bill of Material (SBOM) development and maintenance for the purposes of vulnerability monitoring. + Possess… more
- Medtronic (Mounds View, MN)
- …and executes biostatistical components of plans for clinical research and development projects that establish the conditions essential for determining safety, ... to the life cycle of the product. + In development -phase projects, prepares the statistical component of protocols which...guidelines for clinical trials and medical devices (eg, ISO, MDD/ MDR ). + Prior experience in FDA and/or global regulatory… more
- Kelly Services (Irvine, CA)
- …of the pipeline, product portfolio and business needs; + May serve as the clinical representative on a New Product Development team; + May be responsible for ... development of Post- Market Clinical Follow-up (PMCF) Plans and Reports; + May...(ie, CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR , MEDDEV, ). + Clinical/medical background a plus. +… more
- J&J Family of Companies (Irvine, CA)
- …extensions, etc, including during sponsor regulatory inspections; + Serves as the clinical representative on a New Product Development team; + Is responsible for ... development of Post- Market Clinical Follow-up (PMCF) Plans and Reports; + Conducts...(ie, CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR , ). + Clinical/medical background is a plus. Johnson… 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
- Medtronic (Mounds View, MN)
- …Day in the Life** In this onsite role, you will contribute to the development , testing, and analysis of Leads, Catheters, Devices, and Instruments for cardiac pacing ... other duties may be assigned: + Contribute to the development of design solutions that address broad development...and design optimization techniques + Knowledge of FDA and MDR regulations **Physical Job Requirements** The above statements are… more
- Medtronic (Fridley, MN)
- …evidence * Generate product analysis reports * Provide support with the development of procedures, processes, tools, and techniques for performing product analysis. ... regulations: FDA 21 CFR Part 820, EU 217/745 (EU MDR ) + Familiarity with these standards: ISO 13485, ISO...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Zurich NA (Washington, DC)
- …Security Lead Generation Specialist 127084 **Cyber Lead Generation Specialist (Sales Development Representative )** **Location:** [Remote or St. Louis, MO ... Full-Time SpearTip is a cybersecurity firm specializing in Managed Detection & Response ( MDR ), Incident Response (IR), and Advisory Services. Our mission is to help… more
