- Amrize (Beech Grove, IN)
- …business objectives. + Implements and maintains predictive / preventative maintenance programs, ISO 9001 & 14001 programs. + Incorporates and sustains a strong ... but not limited to, Standard Work, Stigma, Reliability Centered Maintenance, 5S, ISO 9001 & 14001, FTA, Kaizen, and 8D. **Additional Requirements:** + Successful… more
- Nanobiosym, Inc. (Cambridge, MA)
- …+ Support regulatory and quality processes with a focus on FDA and ISO 13485 compliance. Minimum Qualifications: + Master's Degree in Electrical Engineering + 5-10+ ... Strong understanding of compliance standards in regulated industries (eg, FDA, ISO 13485). + Proven track record of delivering production-quality PCBs-from prototype… more
- Nanobiosym, Inc. (Cambridge, MA)
- …a BSL-2 or BSL-2+ facility preferred but not required + Experience working in an ISO 13485 environment, and a working knowledge of ISO documentation & QSR ... requirements preferred but not required + Experience testing and/or developing life sciences products, including meticulous laboratory notebook skills + Must have an understanding of principles of statistics relevant to product testing + Must have an… more
- Burns & McDonnell (San Diego, CA)
- …using AFT products, Ceaser II, etc. Modify and review production drawings, 3D Model, ISO drawings, etc. for a variety of projects including, but not limited to ... bid evaluations and recommend vendors. Review production drawings, 3D Model, ISO drawings, etc. Work closely with other disciplines (Piping, Elelctrical, I&C,… more
- Tri-Mack Plastics (Bristol, RI)
- …accountability and we are committed to meeting customer requirements through our ISO 9001/AS9100 quality management system. PLEASE NOTE - Applicants must be ... the shift to ensure compliance with all quality systems and adherence to ISO requirements including, but not limited to first piece inspection and in process… more
- ARTIDIS (Houston, TX)
- …work instructions (WIs), and test plans in compliance with FDA regulations and ISO 13485 standards. + Provide on-site support and troubleshooting for clinical and ... and quantitative data analysis. + Familiar with medical device operations, ISO 13485, FDA guidelines, CE Marking, and international regulatory frameworks. +… more
- Envista Holdings Corporation (Brea, CA)
- …process and process changes. + Maintains a working knowledge of FDA GMP, ISO 13485 standards and other applicable standards. + Documents data obtained during all ... medical device industry. + FDA Quality System Regulation Part 820 and ISO 13485 experience. + Certified Quality Engineer preferred. **SKILLS & QUALIFICATIONS:** +… more
- Stryker (Cary, IL)
- …design and development. + Familiarity with developing packaging systems compliant with ISO , ASTM, ISTA, or USP standards. + Experience with packaging verification ... or combination product packaging. + Familiarity with sterile packaging systems and ISO 11607 requirements. + Knowledge of FDA regulations (21 CFR 820/211) and… more
- BorgWarner Inc. (Arden, NC)
- …and automation networks (Ethernet/IP, PROFINET). + Experience with safety systems and standards ( ISO 13849, ISO 26262, SIL). + Proficiency in electrical CAD ... tools (AutoCAD Electrical, EPLAN). + Excellent leadership, communication, and project management skills. + Ability to manage multiple projects and prioritize in a fast-paced environment. + Liason between utility supply company and facility/plant leadership to… more
- Amgen (Thousand Oaks, CA)
- …ensuring Procurement deliverables adhere to regulatory requirements (eg, GLP, GMP, ISO ) and implement quality control systems, including audits, inspections, and ... and technologies. + Familiarity with industry standards and regulations (eg, GLP, GMP, ISO , OSHA). + Proven track record to drive value in a procurement environment… more