- Philips (Plymouth, MN)
- …a Senior Program Manager, you will lead high-impact programs that advance our medical device portfolio, elevate product performance, strengthen product quality & ... compliance , and deliver meaningful outcomes for patients and providers...product development, lifecycle management, and global execution across multiple medical device portfolios. + Develop and implement… more
- Zimmer Biomet (Norfolk, VA)
- …leader and Management Representative responsible for directing the quality function a medical device design and manufacturing site. Utilizes quality statistics ... QMSR, GMP, ISO and other relevant regulatory requirements as applied to medical device development, manufacturing and distribution. + Demonstrated independent… more
- BD (Becton, Dickinson and Company) (Covington, GA)
- …shall provide a leading Product & Process Design role in planning and execution of medical device projects for the Urology and Critical Care (UCC) Business Unit. ... This candidate will have a passion for developing robust, well thought-out medical device assembly equipment/processes that optimize for business success through… more
- ManpowerGroup (Savannah, GA)
- Our client, a leading organization in the medical device manufacturing industry, is seeking a dedicated and experienced Quality Engineer to join their team. As a ... 7-10 years of experience in quality engineering within the medical device industry. + Significant experience with...efforts. + Engage in meaningful projects that impact regulatory compliance and product quality. + On-site role supporting a… more
- Medtronic (Northridge, CA)
- …Quality Engineering related to manufacturing Site Quality. Plan, coordinate, and execute Medical Device standards activities to ensure the safety and reliability ... FDA QSR (Quality Systems Regulations), ISO13485, ISO14971, ISO11135, ISO11737, MDD ( Medical Device Directives) 93/42, AIMDD (Active Implantable Medical… more
- Philips (Murrysville, PA)
- …years' experience in Supplier Quality Engineering within highly regulated product environments ( Medical Device preferred), with a focus on supplier selection, ... SPC, SCAR's, SICR, CAPA, Remediation etc. + You have detailed knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts… more
- Microsoft Corporation (Redmond, WA)
- …hardware and software. As an **Principal Software Engineering Manager** for the Open Device Partnership (ODP) program, you will lead a team of engineers focused on ... OEMs, and internal engineering teams to define technical strategy, ensure compliance with Microsoft standards, and influence industry-wide best practices. ODP… more
- Lilly (Concord, NC)
- …+ Bachelor's degree in STEM + Experience working in the pharmaceutical or medical device industry in QA roles + Previous batch disposition experience ... increase the company's manufacturing capacity in parenteral (injectable) medications, device assembly and packaging operations. This is an exciting… more
- GE HealthCare (Waukesha, WI)
- …and Machine Learning techniques. + Hands-on experience integrating AI Models into medical device products + Experience in developing AI inference pipelines ... design and implementation throughout development cycles. + **Quality & Compliance ** : Apply technical expertise to ensure the quality...for medical device . **Desired Characteristics / Technical Expertise**… more
- Oracle (Boise, ID)
- …Oracle Health Data Intelligence is entering a high-impact phase of **MDR ( Medical Device Regulation)** readiness and **regulatory transformation** . Over the ... risk management activities, and engineering design updates** required for compliance across our AI-enabled population health platform. To support...+ Experience with one or more of: + MDR ( Medical Device Regulation) + ISO 14971 (risk… more