Ravi Tan
Program Director, Pharmaceutical Faculty @North American College Of Pharmaceutical Technology Nacpt Pharma College
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WORK HISTORY
Program Director, Pharmaceutical Faculty @North American College Of Pharmaceutical Technology Nacpt Pharma College
Toronto, ON, CA
Specialized in and delivered pharmaceutical and medical marijuana training programs, ensuring their effectiveness, regulatory compliance, and continued relevance.Selected Accomplishments include: • Incorporated practical, hands-on training components such as laboratory work, production simulations, and quality control exercises.• Managed, mentored, and supported pharmaceutical faculty members, ensuring they had the resources, training, and guidance needed for effective teaching. • Oversaw the design, implementation, and continuous improvement of the pharmaceutical programs, ensuring they met educational standards, regulatory guidelines (eg, FDA, GMP, HACCP, etc.) and institutional policies.• Prepared and delivered the pharmaceutical program aligned with regulatory standards (e.g, FDA, GMP, HACCP, etc.)
EDUCATION
University of Strathclyde
Post Doctoral Fellowship, Radical Chemistry
University of Leeds
Ph.D., Organometallic Chemistry (Analytical Chemistry)
University of Jaffna
BSc.(Hons), First class, Chemistry
ABOUT RAVI TAN
Experienced scientific management professional with extensive background in pharmaceuticals and contract research sectors. Direct new product development (NPD), including active pharmaceutical ingredient (API) and final product (FP) analytical method development, according to Analytical Quality by Design (AQbD) principles. Expert in method development, method validation, method transfer, early development (ED) stability, and product / method life cycle management (PLCM / MLCM) for solid dose generic products. Collaborate with effect among cross-functional teams, external partners, and regulatory agencies to ensure quality, compliance, and timely delivery.A listing of my core competencies includes: Pharmaceutical Drug Development Support Analytical Chemistry Good Manufacturing Practices (GMP) Good Lab Practices Auditing Process Improvement Product Management Team Leadership Resource Planning and budget for development activities CDMO ManagementI am available to discuss new opportunities in the United States or in Canada, please contact me at R••••••••@gmail.com
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