at Aerotek in Memphis, Tennessee, United States
Please call me @ 901-462-2318 ask for Anita Douglas if you have any questions or concerns
Medical Industry knowledge and experience
+ 3 to 5 years experience working in an FDA regulatory environment.
Must be able to explain:
1. Experience implementing processes in FDA or ISO 13485 Medical device QMS.
2. Experience in interpreting, implementing, and communicating on regulatory requirements.
Responsible for providing guidelines for quality assurance processes in compliance with FDA Regulatory environment
Engineering, Microsoft office, Customer service, Hardware, Installation, PowerPoint, Design, Telecommunication, FDA compliance, FDA inspections, medical terminology, audit, blueprint reading, Support
Top Skills Details:
Engineering, Microsoft office, Customer service,Hardware,Installation,Powerpoint,Design,Telecommunication,fda compliance, FDA inspections, medical terminology ,audit, blueprint reading
Additional Skills & Qualifications:
Develops and initiates standards and methods of inspection, testing, and evaluation.
We know that a company’s success starts with its employees. We also know that an individual’s success starts with the right career opportunity. As a Best of Staffing® Client and Talent leader, Aerotek’s people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees. Since 1983, Aerotek has grown to become a leader in recruiting and staffing services. With more than 250 non-franchised offices, Aerotek’s 8,000 internal employees serve more than 300,000 contract employees and 18,000 clients every year. Aerotek is an Allegis Group company, the global leader in talent solutions. Learn more at Aerotek.com.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.