Regulatory Specialist: Average Salary in Longmont, CO in 2024
Find out what the average Regulatory Specialist salary is in Longmont, CO
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How much does a Regulatory specialist make in Longmont, CO?
$89,700
/ Annual
Based on 16 salaries
The average regulatory specialist salary in Longmont, CO is $89,700 per year or $43.13 per hour. Entry level positions start at $52,650 per year while most experienced workers make up to $91,893 per year.
The Regulatory Affairs Specialist supports our product teams supporting new product development and lifecycle management. This is a role that would suit an individual interested in developing a career as a regulatory professional and who has interest in supporting the development of in vitro diagnos...
A company is looking for a Regulatory Specialist - Dental Operations. Key Responsibilities:Support external and internal regulatory reporting, surveys, audits and investigations impacting dental operationsMonitor incoming regulations and share regulatory guidance with dental operationsPerform monito...
The Regulatory Specialist will be responsible for ensuring that the claims made for our dietary supplement products are substantiated by scientific evidence and comply with regulatory requirements. We are looking for a positive, driven, and detail-oriented Regulatory Specialist to join our growing t...
Vergent Products, an electronics contract manufacturer, is seeking a full-time Program Manager to provide best in class Program Management. Working with other Program Managers, identify and lead improvement in client experience touch points and program management business processes (ie: Sales order ...
RMI's Climate Intelligence Program is seeking a Manager to join our Carbon Markets Initiative (CMI), which seeks to improve the transparency, efficiency, and quality of carbon credits and accelerating progress towards a 50 percent cut in global greenhouse gas emissions by 2030 and net-zero emissions...
A company is looking for a Director/Senior Director, Regulatory Affairs Advertising and Promotion. Collaborate with cross-functional teams to incorporate regulatory considerations into materialsServe as primary liaison to FDA Office of Product and Drug Promotion (OPDP)Required Qualifications:Minimum...
Key Responsibilities:Focus on clinical regulatory filings and providing strategic and operational leadership on project teamsContribute to IND/CTA and BLA submissions activities for products in developmentDevelop regulatory strategies for assigned programs and communicate with regulatory agenciesReq...
A company is looking for a Senior Manager, Regulatory Affairs. Key Responsibilities:Lead creation and maintenance of Company Core Data Sheets (CCDS) activitiesDrive global implementation of CCDS into country-specific labelingFormulate and drive global technology initiatives for labeling and content ...