Dinesh Khokal

Teaching Pathology & Parasitology, Physiology, Genetics and Bio-statistics & Population Dynamics to undergraduate and masters students

Education

• Doctor of Philosophy - PhD National University of Singapore (1990 — 1995)
• Certificate in Healthcare Policy and Governance Healthcare College, Ministry of Health Holdings Pte Ltd (2013 — 2013)
• Certified Biomedical Auditor (CBA) Americal Society for Quality (ASQ) (2007 — 2007)
• Certified Quality Auditor (CQA) American Socity for Quality (2006 — 2006)
• Certificate in Clinical Trial Management SingHealth (2006 — 2006)
• Master's degree The University of Agricultural Sciences, Bangalore (1980 — 1982)
• Bachelor's degree The University of Agricultural Sciences, Bangapore (1976 — 1980)

Companies

• Director, External Affairs, Corporate Quality, JAPAC & Intercontinental Amgen (2017)
• Director, Therapeutic Products Branch, Pre-Marketing, Health Products Regulation Group Health Sciences Authority, Singapore, Ministry of Health (2013 — 2017)
• Regulatory Consultant (Senior CMC Assessor), Generics & Biosimilars Branch Health Sciences Authority, Singapore (2008 — 2013)
• Regulatory Consultant (Senior CMC Assessor), Pharmaceuticals & Biologics Branch Health Sciences Authority, Singapore (2008 — 2009)
• Senior GMP Auditor, Manufacturing & Quality Audit Division Health Sciences Authority, Singapore (2007 — 2007)
• Site Quality Control Manager A-Bio Pharma Pte Ltd (Biotechnology) (1999 — 2007)
• Senior Scientist, Molecular Biology & Expression Eng Group, Bioprocessing Technology Institute (BTI) A*STAR - Agency for Science, Technology and Research (1999 — 1999)
• Manager & Senior Scientist *Specialty Laboratories Inc, CA, USA (Quest Diagnostics * (1996 — 1999)
• Post-Doctoral Researcher National University of Singapore, Faculty of Science, Department of Biological Sciences (1995 — 1996)

Skills

• Regulatory Requirements
• Cell Culture
• Analytical Chemistry

Other

Protein Chemistry, Quality Auditing, 21 CFR Part 11, ISO 13485, Medical Devices, Laboratory, Quality System, CAPA, Drug Development, HPLC, Chromatography, Biochemistry, Sop, V&V, Clinical Trials, Clinical Development, Quality Control, Microbiology, SOP, DNA, Regulatory Submissions, Lifesciences, FDA, Vaccines, GLP, Hardware Diagnostics, R&D, Biopharmaceuticals, Life Sciences, Technology Transfer, Validation, Biotechnology, Molecular Biology, Regulatory Affairs, GMP, Pharmaceutical Industry