- Sargent & Lundy (Pittsburgh, PA)
- …to directly apply your expertise in power electronics ( FACTS /SVC/STATCOM) in a role of FACTS Subject Matter Expert . This position will be based in ... SME you will support a wide range of FACTS projects providing technical leadership. Project tasks may include...be responsible for proactively guiding the business related to FACTS device standards, codes, designs and other… more
- Philips (Murrysville, PA)
- …phase and provide regulatory guidance throughout design and development. + Act as a Regulatory Subject Matter Expert ( SME ) on various aspects and provide ... with a primary focus on Software as a Medical Device (SaMD) for our Sleep & Respiratory Care products...evaluations, corrections and removals and CAPAs as a regulatory SME . + Review labeling, marketing materials, and claims substantiation… more
- Philips (Murrysville, PA)
- The Senior Quality Lead-Quality Compliance acts as Subject Matter Expert ( SME ) for non-conformance, driving non-conformance reduction and process ... Serve as best practice/quality resource within your own discipline or as technical expert on functional or cross-functional teams/projects. You also act on a global… more
- Philips (Murrysville, PA)
- …assessments, monitoring, training, and close-out activities. + Serves as a key resource and subject matter expert for study sites and investigators, offering ... years of experience in execution of clinical research in the medical device industry (preferred), pharma, biotech, academia, or government research required. + Your… more
- Philips (Murrysville, PA)
- …ensuring data quality, adherence to budgets, timelines, and regulatory standards. + Acts as a subject matter expert on GCP, ISO, FDA, and global regulatory ... in a healthcare setting and/or supporting clinical research and monitoring medical device trials with a sponsor or CRO. You have people leadership experience.… more
- Philips (Murrysville, PA)
- …governance meetings, provide clinical insights for consistent decision-making, and serve as a subject matter expert in post-market surveillance activities to ... Affairs or Medical Safety/Medical Affairs Risk Management in Meical Device industry. Prior hands-on bedside/clinical experience required. 1+ years of… more