Gary Bendik
Director, Business Development & Operations @Pharmeng Technology
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WORK HISTORY
Director, Business Development & Operations @Pharmeng Technology
Toronto, ON, CA
Responsible to create new and support our existing client relationships/opportunities within the Canadian region. Additional responsibilities include development and implementation of PharmEng Technology global and regional Business Development and Operations strategies including technical leadership and support for consultancy staff.
EDUCATION
Brock University
Bachelor of Science (B.Sc.)
ABOUT GARY BENDIK
As a dynamic pharmaceutical industry professional, my passion is to lead with heart and science. Throughout my career, I have had the privilege of working with several high performance teams to help small emerging to large multinational organizations bring their life-changing medicines, goals and objectives into existence. Builder of strong safety and quality cultures, I am driven with the perpetual desire for continuous improvement while providing pragmatic, value-added solutions in highly competitive and complex environments. The need today has never been greater for leaders in the pharmaceutical/biotech industry to establish a strong connection to our patients and local communities. For me, this essential element energizes, guides, motivates and provides true fulfillment in our unified effort to make our World a healthier, cleaner and safer place. Career Highlights:Mylan (Formerly Genpharm Inc.)*Oncology facility start-up experience; formulated and scaled first oncology drug product for companyPatheon (part of ThermoFisher Scientific)* 3-time co-recipient of Trifecta Award for exceeding EBITA, On-Time Delivery and Right-First-Time targets* Principal consultant for South Korean firm to develop and oversee Quality by Design (QbD) program* Organized and led first STEM challenge with over 100 Grade 5 and 6 studentsPharmEng Technology* Led development of Drug Substance/Drug Product Quality Risk Assessments and Tech Transfer documents for leading Canadian biotech firm in the neurodegenerative medicines space* Spearheaded FDA re-inspection preparation team for major OTC firm resulting in lifting of import ban* Authored first Preventative Control Plans for two of Canada\'s largest cannabis firmsExpertise:Solid/Liquid Drug Product Formulation and Technology * Plant Operations * Regulatory cGMP and PAI Audit Preparation * Process Development and Optimization * Drug Product Regulatory Submissions * Validation * Tech Transfer * Quality Risk Management * Quality by Design (QbD)* Lean-Six Sigma Methodologies * Talent Development * Product Lifecycle Management * GxP Documentation * Internal Quality Audits * Business Development * RFQs, Proposals/Contracts
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