Summary
Websites
Skills
Work History
Education
Certification
Languages
Additional Competencies
Overview
Generic

Jimmy Olayinka

GTA,ON

Summary

Experienced Analytical Chemist and Biochemist with a strong background in qualitative and quantitative research and testing. Skilled in content uniformity testing, dissolution profile testing, API label claim testing, identification testing, finished product stability testing, certificate of analysis testing (CofA), chromatography techniques (HPLC, TLC), chemical and biochemical ASSAYS using (UV-VIS) spectrometry, equipment calibration, method development and validation using pharmacopeias (USP). Proficient in applying good manufacturing practices (cGMP and GMP) to conduct analytical research and performing out-of-specification (OOS) procedures such as root cause analysis investigations and implementing corrective and preventive actions (CAPA).

Skills

  • Proficient Analytical (Qualitative & Quantitative) Research Techniques
  • Chemical, Biological & Biochemical ASSAY Techniques
  • Strong Understanding of SOP Implementation
  • Methods development, Audit and Validation ensuring (ALCOA)
  • Proficient in Pharmaceutical Laboratory Techniques
  • In-depth Knowledge of Instrumental Analysis Methods
  • Advanced Chromatography & Spectrometry Techniques [TLC, UV-VIS and IR]
  • Expertise in HPLC Techniques
  • Solid Understanding of Good Manufacturing Practices (GMP, cGMP)
  • Instrument and Apparatus Calibration & Verification
  • Good documentation practices [GDP] & Quality Assurance Review
  • Karl Fischer Analysis & Profile Dissolution Testing

Work History

Quality Assurance and Control - Postgraduate Research Student

Academy of Applied Pharmaceutical Science AAPS
04.2024 - 04.2025
  • Performed over 50 standard and proprietary testing on pharmaceutical drugs (A.P.I) such as (identification testing, uniformity and stability testing), Chemical analysis of the raw materials using chromatography techniques such as (HPLC,TLC), (UV-VIS), Fourier transform Infrared spectroscopy techniques (FTIR) and others
  • Prepared and standardized test solutions and reagents also evaluated samples against standards to ensure accuracy
  • Validated over 50 pharmaceutical label claims via qualitative and quantitative analytical ASSAY testing on the active pharmaceutical ingredients (API) using HPLC, UV-VIS spectrophotometer and other testing such as dissolution, uniformity testing
  • Strict adherence to pharmacopeias specifically (USP), and in house standard operating procedures(SOP)
  • Maintained appropriate GMP and GLP standards with quality documentation and records for regulatory affairs conformance
  • Calibrated, validated and verified laboratory equipment/apparatus and documented readings and adjustments to improve instrumentation accuracy
  • Performing out of specification root cause analysis on over 20 test samples and products that deviated from their standard limits and initiating a corrective action and preventive actions (CAPA) to avoid future deviations

Analytical Research Chemist

JFT Global Pharmaceutical Industries LTD
01.2020 - 02.2022


  • Conducted over 100 routine chemical analysis, quality control analysis and other ASSAYs on raw materials, in process and finished products using in house standard operating procedures (SOPs) with United State Pharmacopoeia (USPs)
  • Assisted in the development of comprehensive quality control plans, methods development and validations, outlining procedures and guidelines for inspectors and maintained accurate documentation of experimental procedures and results in accordance with SOPs
  • Participated in internal audits to verify adherence to established quality management systems and identify opportunities for enhancement
  • Inspected incoming and outgoing materials for accuracy and quality, demonstrated proficiency in using laboratory equipment and adhering to safety protocols
  • Identify and report out of specification and conformance issues to supervisors and other departments, perform root cause analysis to identify defects and deviations and resolve (OOS) deviations using a corrective analysis and preventive actions procedures (CAPA) to improve products quality standards
  • Conducted training sessions for the production team member on proper GMP standard procedures, ensuring an accurate and consistent GMP approach across the team

Biochemistry Lab Assistant

Ladoke Akintola University of Technology
09.2016 - 08.2018


  • Conducting laboratory biochemical research experiments such as researching biological effects and toxicity of 5 different types of herbs and pharmaceutical drugs on body tissues and organs (brain, hearts, liver, pancreas, kidney)
  • Analyzing samples collected from experiments using Enzyme Assays and Bioassays techniques
  • Interpreting the data collected from experiments accurately and maintaining accurate documentation and records of all test performed
  • Collaborate with other researchers, technicians, and faculty members to share knowledge and expertise also assist in compilation and tabulation of data providing preliminary analysis
  • Assembling, calibrating, operating and qualifying for use varieties of laboratory equipment (instrumental and biological laboratory equipments)
  • Presenting and reporting research findings to internal and external stakeholders such as project coordinators and scientists

Education

Post Graduate Diploma - Quality Assurance & Quality Control

Academy of Applied Pharmaceutical Science
Toronto, ON
09-2025

Bachelor of Technology - Biochemistry

Ladoke Akintola University of Technology
Nigeria
03-2018

1 Year Credit Courses - Biotechnology

Loyalist College of Applied Arts And Technology
Belleville, None

Certification

  • GMP (Good manufacturing practices)
  • Pharmaceutical laboratory techniques (PLT) certificate
  • HPLC (High performance liquid chromatography) certificate
  • RA- regulatory affairs certificate (ICH guidelines, FDA, and Health Canada regulations)
  • Advance Dissolution testing certificate
  • WHMIS certificate
  • Standard First aid and CPR certificate.

Languages

English
Sign Language

Additional Competencies


  • Methods development and validation,(USP pharmacopeias)/ in house methods.
  • Good knowledge of Biochemical ASSAYs (Enzymes and bioassays).
  • Knowledge of laboratory information management systems (LIMS).
  • Advanced Chromatography and Spectrometry Techniques (HPLC,TLC, UV-VIS and IR).
  • Instrument and Apparatus Calibration/Verification (balance, Ph meter, others).
  • Good documentation practices(GDP), Document review, audit and Validation ensuring (ALCOA).

Overview

9
9
years of professional experience
1
1
Certificate

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Jimmy Olayinka