- Medtronic (Northridge, CA)
- …As Principal Regulatory Affairs Specialist , you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide ... Medical Devices Directive (93/42/EEC) and European Medical Device Regulation 2017/745 + Experience with...skills in areas of regulatory pathways, risk-benefit analysis, and quality assurance internally and external with respect… more
- Paramount (Burbank, CA)
- …tracking devices + Represent the Measurement Operations team in meetings as a domain specialist on data quality assurance + Open bugs as needed and ... 5 years of experience in Software Quality Assurance + Some knowledge of developing QA ...and education. The benefits available for this position include medical , dental, vision, 401(k) plan, life insurance coverage, disability… more
- Actalent (Marina Del Rey, CA)
- … MANAGEMENT SYSTEM FOR THE QUALITY TEAM! APPLY NOW!! Description: The Quality Assurance Specialist will collaborate with stakeholders to develop, ... Quality Management System and its platform. The QA Specialist I will execute risk assessments,...manufacturing processes, or product development in a pharmaceutical or medical device environment. * Solid organizational and… more
- Kelly Services (West Hills, CA)
- Quality Control Technician The Quality Specialist will maintain quality assurance programs, procedures and controls, ensuring that finished ... and/or reviewed to ensure they meet medical device requirements and are of the highest quality...+ The Product Release Specialist Engineer I, QA will ensure quality and compliance and… more
- Stantec (Los Angeles, CA)
- …practical designs. + Provides contract documents that meet required codes and quality assurance standards. + Learning/Maintaining and Expanding Technical Skills ... Project Designer/Security Specialist , ICT Consulting - ( 24000054 ) **Description**...for the built environment, including pathway drawings, low voltage device and telecommunications outlet plan drawings, systems single line… more
- Envista Holdings Corporation (Brea, CA)
- …evaluations meet all applicable regulations and guidelines, with strong focus on the new Medical Device Regulation (MDR) and FDA IRB studies. He or she ... **Job Description:** The **Regulatory Affairs Specialist ** will be responsible for establishing, coordinating, and...in clinical evaluation that are complaint to the new Medical Device Regulation (MDR) and/or FDA IRB… more
- Stellant Systems (Torrance, CA)
- …functions of the below + Contract Compliance + Flow Down requirements (Internal/External) + Quality Assurance Program Plan + Programs Review / Meetings + Program ... **Overview** **Job Title:** Quality Engineer **Internal Job Title:** Specialist ,...Range:** $80,000 - $120,000 DoE **Benefits:** Comprehensive benefits package, medical /dental/vision, 6% match on 401K, competitive PTO, 9/80 work… more