Careers in Food and Drug Law

Job Seekers, Welcome to FDLI Career Center
Search Filters
Use this area to filter your search results. Each filter option allows for multiple selections.
Search Results: 128 Jobs
Save Agent
Loading... Please wait.
NEW! NEW!
NEW! NEW!
Vicarious Surgical Logo
Vicarious Surgical

Waltham, Massachusetts

NEW! NEW!
Abbott Logo
Abbott

Milwaukee, Wisconsin

NEW! NEW!
Vicarious Surgical Logo
Vicarious Surgical

Waltham, Massachusetts

NEW! NEW!
Vicarious Surgical Logo
Vicarious Surgical

Waltham, Massachusetts

NEW! NEW!
Abbott Logo
Abbott

St. Paul, Minnesota

NEW! NEW!
NEW! NEW!
CVS Health Logo
CVS Health

Blue Bell, Pennsylvania

Johns Hopkins University Logo
Johns Hopkins University

St. Petersburg, Florida

Wayne State University Logo
Wayne State University

Detroit, Michigan

Abbott Logo
Abbott

St. Paul, Minnesota

Abbott Logo
Abbott

Los Angeles, California

Abbott Logo
Abbott

Santa Clara, California

Abbott Logo
Abbott

Detroit, Michigan

Abbott Logo
Abbott

Austin, Texas

Abbott Logo
Abbott

New York, New York

Abbott Logo
Abbott

Austin, Texas

FDA Center for Devices And Radiological Health (CDRH) Logo
FDA Center for Devices And Radiological Health (CDRH)

Silver Spring, Maryland

Abbott Logo
Abbott

Austin, Texas

U.S Food and Drug Administration, Center for Devices and Radiological Health Logo
U.S Food and Drug Administration, Center for Devices and Radiological Health

Silver Spring, Maryland

Abbott Logo
Abbott

St. Paul, Minnesota

Yale University Logo
Yale University

New Haven, Connecticut

Loading... Please wait.
Quality Specialist
A medical device company, located northeast of Pittsburgh, PA, is seeking a Quality Specialist. Responsibilities: Responsible for maintaining a Current Good Manufacturing Practice (cGMP) compliant Quality Management System for a Medical Device manufacturer's implemented systems, processes, equipment and materials compliance to ensure the Quality System is established and maintained in accordance with FDA 21 CFR 820, cGMP, MDR 2017/745, and ISO 13485 requirements. Track, document, and report any changes in, or improvements to, the Quality System. Inspect quality processes, products, device history records, and personnel in all production areas regularly to ensure compliance. Perform trend analysis on production data. Investigate and


This job listing is no longer active.

Check the left side of the screen for similar opportunities.
Loading. Please wait.