- Lockheed Martin (Orlando, FL)
- …CM processes and procedures that meet organizational and industry standards, such as ISO 9001, CMMI, or ITIL \* Assist with control changes to products, services, ... Waterfall \* Familiarity with industry standards, such as SEI CMM and ISO 9000 **Security Clearance Statement:** This position requires a government security… more
- Hologic (Louisville, CO)
- …Degree. + Expertise in FDA Quality System Regulations, especially Design Control requirements, ISO 13485, and Medical Device Directive. + Familiarity with ISO ... 14970, IEC 60601, IEC 62366, and EN 62304. + Experience with managing multi-source demands for project and product support, fostering an effective team environment. + Experience with Oracle or Agile is beneficial. + **Skills** : + Familiarity with Usability,… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …and provide training + Oversee the developing and implementing of the ISO 14001 requirements + Program development and progress reporting + Identification, ... experience in an industrial facility setting focused on implementing and sustaining ISO 14001 certification as well as other Environmental programs. + Depending on… more
- Insight Global (Irvine, CA)
- …DV workflows end-to-end. - Deep familiarity with relevant medical device standards (eg, ISO 13485, ISO 10993) and understanding how they impact DV requirements. ... - Strong communication and collaboration skills with design, quality, and cross-functional engineering teams. - Highly organized, reliable, and comfortable operating with a "service mindset" in support of product development teams. - Experience with wearable,… more
- Caris Life Sciences (Phoenix, AZ)
- …+ Maintain compliance to all applicable regulatory requirements (CLIA, NYS, CAP, ISO , FDA, IVDD, etc.) with regards to laboratory instrumentation calibration and ... years of experience working in a regulated environment (CAP, CLIA, NYS, FDA, ISO , etc.) or Bachelor's degree in a biological science, engineering, or similar field.… more
- Cretex (Coon Rapids, MN)
- …set-ups as required + Support and comply with the company Quality System, ISO , and medical device requirements + Read, understand, and follow work instructions and ... equipment when required - Supports and complies with the company-s Quality System, ISO , and medical device requirements - Completes all other work duties as assigned… more
- Cummins Inc. (Frankfort, KY)
- …**Maintain Compliance and Traceability** Your work supports adherence to international standards ( ISO 17025, ISO 9001, IATF 16949), ensuring traceability and ... audit-readiness across all calibration activities. **Empower Teams Through Training and Support** By training lab personnel, apprentices, and customers, you'll build technical competency and foster a culture of precision and accountability. **Enhance System… more
- Sodexo (MA)
- …leaders across multiple functions and locations. + Advanced working knowledge of ISO 14001 and ISO 45001, with demonstrated experience implementing management ... systems. + Strong analytical skills and the ability to use data to proactively manage risk and drive decision-making. + Highly organized, detail-oriented, and proficient in Microsoft Office with the ability to manage complex programs and competing priorities.… more
- Cretex (Brooklyn Park, MN)
- …integration practices. + Support and comply with company Quality System, ISO 13485, and medical-device regulatory requirements. Qualifications + Bachelor's Degree in ... technology, custom machinery, and cost-reduction initiatives. + Experience in an ISO 13485/GMP regulated environment. + Engineering experience with medical devices… more
- Wolters Kluwer (Philadelphia, PA)
- …while ensuring strict compliance with global regulatory standards such as FDA, EU MDR, ISO 13485, and IEC 62304. They are responsible for creating and managing the ... risk assessments, testing, etc.). + Demonstrated experience working under a formal QMS ( ISO 13485, 21 CFR 820) + Experienceworking with aneQMSand other tooling for… more