- Cognizant (Chicago, IL)
- …Global Pharmaceutical market and industry, including BioTech, Medical Device , Traditional Rx, enabling technologies and regulatory /compliance in the ... **Experience Partner - Life Sciences (Pharma / BioTech / Medical Device )** **Associate Director - Chicago/Midwest Remote** **Who we are:** We are Cognizant… more
- Henry Ford Health System (Detroit, MI)
- …+ Minimum of eight (8) years of experience in information security with focus on medical device security. + Minimum of three (3) years of management experience ... Certification. + CEH Additional Information + Organization: Corporate Services + Department: Ascension MEDICAL DEVICE SECUR + Shift: Day Job + Union Code: Not… more
- AbbVie (Pleasanton, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- AbbVie (Irvine, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- Pfizer (Kalamazoo, MI)
- …/Combination Products. Supports the creation, development and monitoring of Quality and Regulatory Compliance strategies for medical devices and combination ... and continual improvement. + Development, implementation and monitoring of Quality and Regulatory Compliance strategies for medical devices and combination… more
- J&J Family of Companies (Santa Clara, CA)
- …is a plus. + Understanding of clinical trial design, GxP principles, and FDA/EMA regulatory requirements, particularly for medical device submissions such as ... aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease...programmer with a strong interest in clinical data analysis, regulatory processes (such as PMA or 510(k) submissions), and… more
- RWJBarnabas Health (Newark, NJ)
- Director Patient Care Ventricular Assistive Device (VAD) ProgramReq #:0000189067 Category:Professional / Management Status:Full-Time Shift:Day Facility:Newark Beth ... Israel Medical Center Department:Cardiac Recovery Room Pay Range:$125,000.00 - $175,000.00...NJ 07112-2027 Job Title: Director Patient Care Ventricular Assistive Device (VAD) Program Location: Newark Beth Israel Med Ctr… more
- Ricoh Americas Corporation (Indianapolis, IN)
- …in a technical field and 3+ years of experience in manufacturing quality operations medical device industry. + ISO 13485 experience required + Experience working ... such registrar/notified bodies with support from Director level Quality & Regulatory personnel. Job Duties and Responsibilities **Quality System Development and… more
- Lilly (Pleasant Prairie, WI)
- …are determined to make life better for people around the world. The Device Assembly and Packaging (DAP) Operations Sr Director is responsible to provide leadership ... Modes Effect Analysis (FMEA). + This role has direct interaction with Regulatory Agencies during site inspections. + Understand and influence the manufacturing… more
- Abbott (Santa Clara, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... potential impact on the business **Preferred** **Qualifications** + Experience in the medical device industry preferred + Experience with clinical trials… more