Regulatory Affairs Manager


Greenville, SC

Industry: Patient Care


8 - 10 years

Posted 407 days ago

This job is no longer available.

Develop regulatory and CMC strategy.  Manage support labeling, FDA guidelines, project and product development teams.  Prepare and approve drug products, QA, preparation and filing of regulatory submissions, compliance. Must have 8+ years’ appropriate experience working in a GMP environment, focusing on pharma product development. May consider a Director level candidate for more $$. MS or PhD(CHM)(BIOLOGY) or related.

For almost 40 years, Bryant Associates, a nationally recognized, global executive search firm, has successfully matched clients and candidates in a broad spectrum of industries. Our client list includes major Fortune level companies as well as smaller entrepreneurial organizations. Although we are a generalist recruiting firm and work across all disciplines, our practice has a targeted marketing and sales specialty. Bryant Associates, Inc. was founded by Richard Bryant, an accomplished industry leader, whose track record and executive placement awards identify him as an experienced recruiting professional. We feel that our past performance and number of years in business make a difference, but we also understand that each assignment requires us to begin anew. Our recruitment philosophy is basic and our operating process is simple...we listen, respond and continually strive to deliver added value.

$90K - $110K