- Beckman Coulter Diagnostics (Miami, FL)
- …and standards including compliance with Food & Drug Administration (FDA), Medical Device Single Audit Program (MDSAP), ISO13485, European Union Medical Device ... Directives (MDD), and In-Vitro Medical Device Regulation (IVDR) as well as all other applicable global regulatory requirements.Maintain oversight, tracking, metric reporting and escalation of issues while providing consultation and support for the… more
- Cytiva (Miami, FL)
- …or project engineering role, preferably in healthcare manufacturing or medical device production.2+ years experience with regulatory standards and quality systems ... concise language for a non-technical audience.Working in Pharmaceuticals or Medical Device industryExperience with Veeva & Magic systemsCytiva, a Danaher operating… more
- Raytheon (Andover, MA)
- …Sklearn, Matplotlib)Advanced degree in STEM or statisticsSolid state device physics knowledgeSemiconductor wafer fab processing experienceStrong problem-solving ... skillsProject management skillsFailure analysis experience with SEM, FIB, STEM, etc.Experience in RF fieldExperience with lab tools such as probe stations, curve tracers, Keithly/Keysight equipmentExperience with related industry standards such as JEDEC,… more
- Raytheon (Mckinney, TX)
- …Windchill and the Common PDM system, ASME BTH-1 (Below-the-Hook Lifting Device Design)Active and transferable DoD Security ClearanceWhat We OfferOur values drive ... our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Safety, Trust, Respect, Accountability, Collaboration, and Innovation.Learn More & Apply Now!Please consider the following role type definition as you… more
- Beckman Coulter Life Sciences (Indianapolis, IN)
- …development, manufacturing and / or quality systems (ISO 9001), medical device (ISO 13485), pharmaceutical, related life sciences or other regulated industries.It ... would be a plus if you also possess previous experience in:Ability to identify, develop and execute quality system, product and process improvements. Driving change cross functionally across multi-site operations.Certified Software or Quality Engineer (SQA)… more
- Cytiva (Miami, FL)
- …be a plus if you also possess previous experience in:Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949#LI-OnsiteJoin our winning team ... today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.For more… more
- Cytiva (Miami, FL)
- …be a plus if you also possess previous experience in:Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949Speaking fluent SpanishCytiva, a ... Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher… more
- Beckman Coulter Diagnostics (Miami, FL)
- …if you also possess previous experience in: Experience in IVD Medical device or Pharmaceutical ManufacturingASQ CertificationThe salary range for this role is ... 100K-115K. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.This job is also eligible for bonus/incentive pay.We offer comprehensive… more
- Cytiva (Miami, FL)
- …or Manufacturing Operations within Life Sciences, Biotechnology, Medical Device , Biopharma, or other FDA or EPA-regulated manufacturing environments.Possess ... a minimum of 4 years of leadership experience, with senior leadership roles in QA, Operations, or Quality Engineering preferred.Regulatory and Quality Expertise: Strong knowledge of ISO standards, FDA regulations, cGMPs, CFR requirements, and quality… more
- Cytiva (Miami, FL)
- …in Quality or Regulatory in a regulated industry (ISO 9001, medical device , or pharmaceutical preferred).Experience with root cause analysis, CAPA management, and ... validation activities (IQ, OQ, PQ).Proficiency in Microsoft Office (Word, Excel, PowerPoint, Project, Minitab, Visio).Knowledge of manufacturing processes, material properties, and product assembly within a regulated environment.Travel, Motor Vehicle Record &… more
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