About the Company:
Our client is a medium sized medical device company focused on surgical devices headquartered in Irvine, CA.
Our client produces and manufacturers an array of products ranging in different Surgical devices
This role will start 9/21, and will go permanent after 6 months.
About the Role:
Working in a large, but collaborative group of QA professionals; you will be responsible for ensuring that processes and work practices are documented and are efficient, effective, and compliant to local, state, federal and international regulations.
You will be a core team member working directly with the Director of QA/RA, and managing a team of QC Inspectors, Quality Engineers, and Quality Specialists.
You will be working in medium to large company, and will be working in a fast paced environment.
Your skills and experience
- Bachelor's degree preferable in engineering, or life science.
- 4-5 years of experience in a regulated QSR environment (medical device, aerospace, or automotive).
- Experience in industrial industries particular working with hygiene/safety, government regulations, operational auditing, and manufacturing operations.
- Validation, and Quality experience a plus.
You are a positive person with great communication skills. You are able to manage employees in a positive, but constructive manner. You are a team player who enjoys working in a cross functional team, and in a collaborative environment. You have strong communication, social skills, and Quality experience in an industrial engineering/regulated environment. You have worked in the medical device, aerospace, or automotive industries, and are interested in a collaborative, multi-functional, and fast paced environment.
Sthree US is acting as an Employment Business in relation to this vacancy.