Experience

Chameleon Communications International

• United Kingdom
• Advertising Services
• 100 - 200 Employee

• Scientific Director

  • Jul 2023 - Present

• Associate Scientific Director

  • Aug 2022 - Jul 2023

• Assistant Scientific Director

  • Oct 2021 - Aug 2022


Six Degrees Medical
• Canada
• Advertising Services
• 1 - 100 Employee
• Medical Writer

  • Oct 2020 - Oct 2021


Catalent Pharma Solutions

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Associate Formulation Scientist

  • Feb 2017 - Aug 2018

  As an Associate Formulation Scientist, I worked within the formulations R&D department and collaborated with other cross-functional teams. I handled 3 to 4 projects within the R&D portfolio at different stages of the product life cycle. I acquired experience working with potent drug substances. My role consisted of designing and executing several pre-formulation and formulation studies based on QbD and DOE principles. I authored and reviewed several study protocols, technical reports and batch… Show more As an Associate Formulation Scientist, I worked within the formulations R&D department and collaborated with other cross-functional teams. I handled 3 to 4 projects within the R&D portfolio at different stages of the product life cycle. I acquired experience working with potent drug substances. My role consisted of designing and executing several pre-formulation and formulation studies based on QbD and DOE principles. I authored and reviewed several study protocols, technical reports and batch documents. Using QbD principles and statistical analysis in product development. I obtained hands-on experience in using bench top encapsulation machines and other equipment used in the soft-gelatin capsule evaluation. Show less As an Associate Formulation Scientist, I worked within the formulations R&D department and collaborated with other cross-functional teams. I handled 3 to 4 projects within the R&D portfolio at different stages of the product life cycle. I acquired experience working with potent drug substances. My role consisted of designing and executing several pre-formulation and formulation studies based on QbD and DOE principles. I authored and reviewed several study protocols, technical reports and batch… Show more As an Associate Formulation Scientist, I worked within the formulations R&D department and collaborated with other cross-functional teams. I handled 3 to 4 projects within the R&D portfolio at different stages of the product life cycle. I acquired experience working with potent drug substances. My role consisted of designing and executing several pre-formulation and formulation studies based on QbD and DOE principles. I authored and reviewed several study protocols, technical reports and batch documents. Using QbD principles and statistical analysis in product development. I obtained hands-on experience in using bench top encapsulation machines and other equipment used in the soft-gelatin capsule evaluation. Show less



Accucaps Industries Ltd.

• Canada
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Associate Formulation Scientist

  • Sep 2016 - Feb 2017

  Performed formulation screens, stability studies, and drug product process development for soft gels. Performed process development to develop robust processes that scale effectively to GMP standards. Designed and executed internal and external client experiments including DOE studies. Authored and reviewed study protocols and technical reports and batch documents. Executed optimization, feasibility, scale-up and stability trials for soft-gel capsules. Designed and executed… Show more Performed formulation screens, stability studies, and drug product process development for soft gels. Performed process development to develop robust processes that scale effectively to GMP standards. Designed and executed internal and external client experiments including DOE studies. Authored and reviewed study protocols and technical reports and batch documents. Executed optimization, feasibility, scale-up and stability trials for soft-gel capsules. Designed and executed several pre-formulation and formulation studies based on QbD and DOE. Show less Performed formulation screens, stability studies, and drug product process development for soft gels. Performed process development to develop robust processes that scale effectively to GMP standards. Designed and executed internal and external client experiments including DOE studies. Authored and reviewed study protocols and technical reports and batch documents. Executed optimization, feasibility, scale-up and stability trials for soft-gel capsules. Designed and executed… Show more Performed formulation screens, stability studies, and drug product process development for soft gels. Performed process development to develop robust processes that scale effectively to GMP standards. Designed and executed internal and external client experiments including DOE studies. Authored and reviewed study protocols and technical reports and batch documents. Executed optimization, feasibility, scale-up and stability trials for soft-gel capsules. Designed and executed several pre-formulation and formulation studies based on QbD and DOE. Show less



Western University

• Higher Education
• 1 - 100 Employee

• Research Assistant

  • Sep 2015 - Mar 2016

  Department of Microbiology and Immunology. Assisted in research on pyroptosis pathways. Department of Microbiology and Immunology. Assisted in research on pyroptosis pathways.

• Validation Specialist

  • Jan 2015 - Jun 2015

  Developed process validation and cleaning validation plans, protocols, IQ/OQ/PQ. Designed cleaning validation studies. Assisted in the execution of process qualification/cleaning validation protocols for production. Wrote Standard Operating Procedures on validation and qualification methods. Performed change control assessments to determine the impact on processes. Provided training specific to validation protocol requirements to the production department. Applied… Show more Developed process validation and cleaning validation plans, protocols, IQ/OQ/PQ. Designed cleaning validation studies. Assisted in the execution of process qualification/cleaning validation protocols for production. Wrote Standard Operating Procedures on validation and qualification methods. Performed change control assessments to determine the impact on processes. Provided training specific to validation protocol requirements to the production department. Applied statistical methods in process validations and equipment qualifications

• Analytical Scientist

  • May 2014 - Dec 2014

  Performed analytical method development, method validation and method transfers. Prepared analytical methods, protocols and reports afor analytical development and validation activities. Performed stability testing in accordance with ICH or other regulatory guidelines. Prepared and implement stability protocols and scheduling. Supported formulation development for analytical testing for stability and validation studies. Performed root cause analysis including OOS and OOT and solved… Show more Performed analytical method development, method validation and method transfers. Prepared analytical methods, protocols and reports afor analytical development and validation activities. Performed stability testing in accordance with ICH or other regulatory guidelines. Prepared and implement stability protocols and scheduling. Supported formulation development for analytical testing for stability and validation studies. Performed root cause analysis including OOS and OOT and solved method related problems. Ensured compliance with local and global regulatory guidelines (e.g. ICH, GMP, GCP and GLP)