- J&J Family of Companies (Orlando, FL)
- …moral character while professionally representing the company. + Comply with all corporate compliance, FDA , medical device , quality standards and ethics. ... Must not be debarred by FDA for work in any Medical Device business. + Establishes and maintains relationships with customers, hospitals, and physicians.… more
- J&J Family of Companies (Birmingham, AL)
- …moral character while professionally representing the company. + Comply with all corporate compliance, FDA , medical device , quality standards and ethics. ... + Must not be debarred by FDA for work in any Medical Device business. + Ability to work in a fast-paced environment while managing multiple priorities.… more
- Family Dollar (Chesapeake, VA)
- …of Quality work experience in FDA regulated industries. (pharmaceutical or medical device industry preferred). + Working knowledge of FDA Quality ... **Family Dollar** ** Quality Assurance Associate** _About Us_ Based in Chesapeake,...job responsibilities for your assigned area(s), ie, OTC drugs, medical devices, dietary supplements, and/or cosmetics, and may be… more
- Hologic (Newark, DE)
- …to commercialization. + **Regulatory Standards:** Familiarity with ISO and FDA quality systems regulations and medical device design and development ... Experience:** + Experienced with ISO and FDA quality systems regulations. + Prior experience in medical... quality systems regulations. + Prior experience in medical device design and development cycles. +… more
- Cordis (Santa Clara, CA)
- …of education and experience preferred + Expertise in the FDA and International Medical Device Quality System Regulations and ISO 13485 + Six Sigma, ... + Ability to comprehend principles of engineering, chemistry, polymers, physiology, and medical device use. **REQUIRED KNOWLEDGE, SKILLS, ABILITIES** + Excellent… more
- Integra LifeSciences (Plainsboro, NJ)
- …treatment pathways to advance patient outcomes and set new standards of care. The **Sr.** ** Quality Engineer - Medical Device / Pharma** will provide Plant ... Administration ( FDA ) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian ...Experience: 6 to 8 years of experience in a Quality Assurance role for medical device… more
- AbbVie (Pleasanton, CA)
- …discipline. Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, ... GD&T + performing daily assigned tasks in compliance with FDA 's Quality System Regulation (QSR), ISO 13485,...MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes… more
- Mallinckrodt Pharmaceuticals (Madison, WI)
- Job Title Director of Operations, Medical Device Requisition JR000015183 Director of Operations, Medical Device (Open) Location Madison, WI Additional ... Locations Job Description Summary Job Description The Director of Operations - Medical Device will provide strategic direction and leadership for all aspects of… more
- US Tech Solutions (San Bruno, CA)
- …align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process Verification, ... NC/CAPA, Audits) and US and International Medical Device Regulations & Regulatory Agencies (eg, FDA ,... Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management… more
- Ricoh Americas Corporation (Indianapolis, IN)
- …Bachelor's degree in a technical field and 3+ years of experience in manufacturing quality operations medical device industry. + ISO 13485 experience ... requirements, and to acquire and maintain the equipment necessary to validate product quality . + Ensures compliance with FDA , HIPAA, and other applicable… more