Director of Regulatory Affairs, PV and Quality Operations @ (July 2016 - February 2021)
Lecturer - Introduction to Clinical Research @ (May 2016 - December 2018)
Regulatory Affairs Specialist @ Actavis Pharma Company (January 2008 - June 2016)
Senior Regulatory Affairs Associate @ PDi PHARMACEUTICALS INC. – Consulting Firm (May 2005 - January 2008)
Consultant for Regulatory Services @ Generic Pharmaceutical Industry “PROFARMA”, Tirana, Albania (January 1998 - January 2005)
Reviewer - Registration Division (Quality Department) @ National Center of Drugs Control (Ministry of Health) - Tirana, Albania (January 1994 - January 2000)
National GMP Inspector, Inspection Division @ National Center of Drugs Control (Ministry of Health) - Tirana, Albania (January 1992 - January 1994)
Etleva Xeka Education
Academy of Applied Pharmaceutical Sciences, Toronto, Canada
Faculty of Pharmacy, University of Tirana, Albania
B.Sc. (Hons) (PHARMACY)
1988-1992
other
Etleva Xeka Skills
Generics
Regulatory Submissions
eCTD
Quality Assurance
Regulatory Strategy
Pharmaceuticals
Public Speaking
Regulatory Requirements
GMP
FDA
CAPA
Management
Change Control
IND
Pharmaceutical Industry
cGMP
ANDA
Regulatory Affairs
Research
Etleva Xeka Summary
Etleva Xeka, based in Richmond Hill, ON, CA, is currently a Associate Director, Regulatory Affairs at Searchlight Pharma Inc.. Etleva Xeka brings experience from previous roles at Searchlight Pharma Inc., Regxia Inc., Seneca College and Actavis Pharma Company. Etleva Xeka holds a 2004 - 2006 Post-Graduate Pharmaceutical "Professional Regulatory Affairs" Diploma @ Academy of Applied Pharmaceutical Sciences, Toronto, Canada. With a robust skill set that includes Generics, Regulatory Submissions, eCTD, Quality Assurance, Regulatory Strategy and more. Etleva Xeka has 1 emails on RocketReach.
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