- Omnicell (Pittsburgh, PA)
- Software Engineering Manager would lead multiple team(s) of software engineers and SDETs to build the Omnicell Device Application Platform and Applications. ... **Essential Functions** In order to work effectively as a Software Engineering Manager, the position is expected to: + Hire, mentor, and lead by influence, a… more
- Merck (West Point, PA)
- …: Demonstrated expertise of technical aspects and interdependencies across DS, DP, Device , Packaging, and Analytical, Regulatory, Quality , and Supply Chain from ... Requirement and Experience:** + Bachelor of Science (BS) Degree in relevant engineering or science fields with fifteen (15) years of relevant experience, or… more
- Philips (New Kensington, PA)
- …fit if:** + You have a minimum of 5+ years' experience within FDA regulated medical device Quality environments, with a focus on CAPA reviews, ... The Senior Quality Engineer-CAPA will play a critical role within...opportunities for improvement. + You have detailed knowledge of medical device regulations, requirements, and standards, such… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …quality management experience or high school diploma with 5 years relative quality assurance or engineering work experience. Knowledge, Skills and Abilities + ... innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and… more
- Envista Holdings Corporation (Quakertown, PA)
- …regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to foster ... problem-solving and cooperation. + Experience and working knowledge of electrical medical device manufacturing (preferred). + Experience with SAP is… more
- Merck (West Point, PA)
- …and Skills: . **Manufacturing** - Injection Molding and Automated Assembly of Medical Device Components. Final Assembly and Packaging of Combination Products. ... and compliance requirements governing development and manufacturing for MDCP (21 CFR Part 4, Medical Device Reporting, ISO 13485:2016, EU Medical Device … more
- Philips (Murrysville, PA)
- …factories while pursuing continuous quality improvement through the application of Quality Engineering practices. **Your role:** + Product Ship Holds & ... right fit if:** + Bachelor's degree required. 5+ years of experience in a medical device or regulated industry (preferred). + Direct inspection engineering … more
- Chemours (Harrisburg, PA)
- …, Biological Science, Toxicology or comparable technical field + 5+ years of medical device regulatory compliance experience with respect to raw material ... components and/or 5+ years' experience assessing risk associated with materials supplied to medical device customers + Familiarity with US medical device … more
- Philips (Mount Pleasant, PA)
- …Improvement techniques and Leadership + Prefer experience in Medical Device , Process Improvement, Continuous Improvement, Design for Quality , CAPA. + ... equivalent. + 2+ years of experience with Bachelor's in areas such as Quality Engineering , Safety Engineering , Process Engineering or equivalent. +… more
- Sanofi Group (Swiftwater, PA)
- …and bring hope to patients and their families. The strategic vision of Sanofi's Global Medical Device and Packaging organization is to lead the industry in ... market auto-injectors, pens, safety syringes, as well as connected medical device technologies, and we are gearing...equipment, printing, and vision control systems. + Knowledge of device and packaging regulations, quality systems, design… more