Director, Global Regulatory Affairs with TEAMS Skills Salary

How much does a Director, Global Regulatory Affairs with TEAMS skills make in the United States? The average salary in the United States is $126,964 as of October 30, 2019, but the range typically falls between $109,987 and $148,418. Skills can impact your salary greatly depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.

Base Salary

Core compensation

$109,987
$148,418
$126,964
Job Openings for Director, Global Regulatory Affairs
Adecco - Fremont , CA
The Adecco Group is a global leader in HR services. Our group connects over 700,000 associates with ... Contact us today to discuss available contract and direct hire positions. Adecco Group provides one ...
Adecco - 4 days ago
Global Medical Device Manufacturing Company - San Jose , CA
Regulatory Affairs Coordinator - Bi-lingual Chinese * Responsible for supporting the implementation of Regulatory Affairs and Quality Assurance systems and procedures relating to Domestic and/or ...
ZipRecruiter - 4 days ago
... a leading global organization providing consulting and training services to the Regulatory Affairs and Quality Assurance functions within the Life Science industry. We are proud of our focus on ...
ZipRecruiter - 8 days ago
Memjet - San Diego , CA
Memjet has global reach and presence. Our Corporate Office is in San Diego, CA, with offices in ... The Regulatory Affairs Project Manager will support Memjet's commercialized and developmental inks ...
ZipRecruiter - 8 days ago
SlingShot Connections - Sunnyvale , CA
... global regulatory submissions/approvals • Provide oversight of third party agency testing (UL, EMC, biocompatibility, sterilization assurance) as required • Perform other duties as required Job ...
ZipRecruiter - Today
... global regulatory submissions, claims substantiation, post market surveillance, and tracking data optimization. These activities are in direct support of product approval for drugs. Responsibilities ...
Postings.com - 7 days ago