- Eliassen Group (Trenton, NJ)
- …strengthen development efficiency * You'll interface with software test to ensure high quality product * You will develop automated unit and integration tests * ... applicable. BIG PLUS: Bluetooth experience & Any industry experience that has FDA requirements OR enterprise level company experience and documentation. There will… more
- Fujifilm (Trenton, NJ)
- …of the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Penn Medicine (Atlantic City, NJ)
- …practice/department in maintaining a patient/customer focus, supports the delivery of high quality care, shares a passion for patient and customer-centered care, and ... reports as requested. + Other / Regulatory: + Ensures compliance with all applicable federal, state, and local regulatory...federal, state, and local regulatory standards (ex TJC, DOH, FDA , HIPAA, HCFA, DPW, LCGME, SCGME, etc) + Flexible… more
- Eliassen Group (Trenton, NJ)
- …develop corrective actions + Ensure all written materials align with company, quality , and FDA guidelines across all manufacturing components **Experience ... further and achieve more with their technology solutions, financial, risk & compliance , and advisory solutions, and clinical solutions. With offices from coast to… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in...held religious belief or other legally required exemption._ _In compliance with the ADA Amendments Act, should you have… more
- US Tech Solutions (Branchburg, NJ)
- …lines as well as critical care. **JOB SUMMARY:** * Responsible for maintaining compliance with FDA , AATB, international and state regulations during the second ... level quality review of all **tissue donor files** for tissue submitted to ensure the safety of **donated human tissue.** * Responsible for the triage and review of… more
- Fujifilm (Trenton, NJ)
- …of the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more