Sr. Product Compliance Analyst
Santa Ana, California
To thrive as a Sr. Product Compliance Analyst, you'll provide expertise in requirements related to paints and consumer goods. You will ensure all items meet compliance standards. This includes authoring and maintaining Safety Data Sheets (S...
15d
| Job Type | Full Time |
a Global Energy Research & Analysis Lead - North America
North Carolina
We are seeking a Global Energy Research & Analysis Lead - North America, to drive the monitoring and analysis of national and regional energy trends with a specific focus on electricity and grids. The role will be based in Washington DC. Th...
15d
| Job Type | Full Time |
a Global Energy Research & Analysis Lead - North America
Washington, D.C.
We are seeking a Global Energy Research & Analysis Lead - North America, to drive the monitoring and analysis of national and regional energy trends with a specific focus on electricity and grids. The role will be based in Washington DC. Th...
15d
| Job Type | Full Time |
Senior Regulatory Affairs Specialist
San Diego, California
Senior Regulatory Affairs Specialist Monday - Friday, 8:30 am - 5:00 pm About the Opportunity The Senior Regulatory Affairs Specialist is responsible for ensuring compliance with all applicable worldwide regulatory requirements and standard...
15d
| Job Type | Full Time |
Montvale, New Jersey
Regulatory Affairs Associate ID 2026-2275 Category Legal Position Type Salaried Remote No Starting From USD $59,000.00/Yr. Maximum Pay Range USD $75,500.00/Yr. Shift Time 40 Overview At Benjamin Moore, we empower our team members to achieve...
16d
| Job Type | Full Time |
FDA Associate - Regulation, Labeling & Marketing (Mid-Level)
Washington, D.C.
Venable LLP's FDA Group seeks a mid-level associate to join its nationally recognized Food & Drug Law practice in the Washington, D.C. office. Venable's Food & Drug Law Group advises leading companies across the food, dietary supplement, me...
16d
| Job Type | Full Time |
Regulatory Affairs Specialist II - Temporary
Irvine, California
Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive. Activities include preparation revision of technical files when needed, update l...
16d
| Job Type | Temporary |
Senior Advisor, Regulatory and Clinical Affairs
Vermont
About Us: How many companies can say they've been in business for over 179 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles ever-changing environments in a fast-paced world, meeting it with cutting edge of ...
17d
| Job Type | Full Time |
Senior Advisor, Regulatory and Clinical Affairs
Kansas
About Us: How many companies can say they've been in business for over 179 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles ever-changing environments in a fast-paced world, meeting it with cutting edge of ...
17d
| Job Type | Full Time |
Senior Advisor, Regulatory and Clinical Affairs
New York
About Us: How many companies can say they've been in business for over 179 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles ever-changing environments in a fast-paced world, meeting it with cutting edge of ...
17d
| Job Type | Full Time |