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Quality Documentation Specialist

Quality Assurance

Santa Barbara, CA

 

 

About Sientra

Headquartered in Santa Barbara, California, Sientra is a diversified global medical aesthetics company and a leading partner to aesthetic physicians. The Company offers a suite of products designed to make a difference in patients' lives by enhancing their body image, growing their self-esteem, and restoring their confidence. Sientra has developed a broad portfolio of products with technologically differentiated characteristics, supported by independent laboratory testing and strong clinical trial outcomes.

 

Our leadership is driven by decades of experience and skill that help bring your goals and aesthetic visions to life. We believe that shared expertise and values are essential components of success. We are seeking exceptionally talented and motivated people to join our team. If you are looking for a career that is both challenging and rewarding, and to work for a company at the forefront of the aesthetic industry, please check out our available opportunities. We look forward to hearing from you!

 

 

Essential Duties and Responsibilities

The Quality Documentation Specialist is responsible for the supervision, coordination and maintenance of all required documentation for in-process and finished devices purchased or manufactured by Sientra.

 

Supervisory Responsibilities

This job has no supervisory responsibilities.

 

 

Requirements (Education, Certificates, Licenses, Registrations, etc.)

 

This description contains the essential functions necessary to evaluate the position. It is not intended and should not be used as an exhaustive list of all responsibilities, skills or efforts.

 

FLSA Status: Non-Exempt

 

 

If you would like to apply for this position, please email your resume to careers@sientra.com.