- 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
- 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
- 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
- Dentsply Sirona (York, PA)
- …EMA, MHRA, TGA, Health Canada) in compliance with 21 CFR Part 803, EU MDR , and other applicable regulations. _Post Market Surveillance Execution_ + Supports a ... to: **Develop faster** - with our commitment to the best professional development . **Perform better** - as part of a high-performance, empowering culture. **Shape… 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
- 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 ... Develop and implement comprehensive marketing strategies to support product launches, market penetration, and portfolio growth in alignment with business objectives.… more
- Medtronic (Minneapolis, MN)
- …partners and global regulatory agencies to introduce products and changes to market . This role involves: + Providing expert advice on regulatory requirements + ... and Canadian submissions for product changes to ensure timely approval for market release. + Review significant regulatory issues with the manager as necessary,… more
- Globus Medical, Inc. (Audubon, PA)
- …ensures compliance with applicable regulatory requirements (FDA QSR, ISO 13485, EU MDR , MDSAP, etc.) and alignment with company objectives for product safety, ... objectives and regulatory requirements. + Provide leadership, mentoring, and development for the Quality Engineering, International Quality, and Sterile… more
- Medtronic (Boulder, CO)
- …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 (Newton, MA)
- …of cybersecurity and the software lifecycle within regulated environments, including design, development , and post- market support. + Experience with cardiac and ... a team of engineers and cross-functional partners to support design, development , and maintenance of software for Affera cardiac electrophysiology systems. By… more
- Medtronic (Santa Rosa, CA)
- …approval to introduce new products (Class II and Class III) to market , provides advice on regulatory requirements, prepares worldwide submissions and negotiates ... provide an opportunity to work on a new product development project for a Class III device that seeks...ensure timely approvals and compliance for clinical studies and market release. Review significant product submissions with manager and… 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...include; CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR , MEDDEV). + Medical device experience highly preferred. +… 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
- Kelly Services (Norcross, GA)
- …seeking a highly skilled Principal, Regulatory Affairs professional to manage pre- market regulatory activities for medical devices, including in vitro diagnostics ... Canada, and EU Notified Body requirements, providing regulatory guidance throughout product development and launch. This position serves as a key regulatory partner… more
- Edwards Lifesciences (Monterey, CA)
- …to support the development of clinical evaluation reports. + Act as representative in core team meetings in the development of regulatory submissions for ... complex medical writing documents/deliverables such as clinical evaluation plans/report, post- market clinical follow-up plans/reports, and Summary of safety and… more
- J&J Family of Companies (Raynham, MA)
- …**Job Function:** R&D Operations **Job Sub** **Function:** Product Development Testing **Job Category:** Professional **All Job Posting Locations:** ... legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary… more