Director, Quality Assurance and Technical Affairs

Opportunity for top-notch individual to be a part of a dynamic Regulatory & Scientific Affairs Department of Consumer Healthcare Products Association, a national trade association located in Washington, DC.  Primary responsibilities include leading projects for Association’s Manufacturing Controls Committee, interfacing with FDA on matters of policy related to cGMP compliance and related issues, organizing educational programs and representing CHPA on joint projects USP, ICH and other important standards-setting organizations.

Qualifications:  M.S. or PhD in chemistry or related field, with 2-5 years’ experience in pharmaceutical analytical chemistry and quality assurance.  Project leadership, ability to manage multiple programs and strong written and oral communications skills are essential.

If you are looking for a competitive salary, excellent working environment and benefits, e-mail resume with cover letter to rmclaughlin@chpa-info.org