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Tolu Oladimeji

@toluoladimeji

Detail-oriented QC Biochemist with expertise in pharmaceutical analysis.

Ireland
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What I'm looking for

I am seeking a role that fosters collaboration and innovation in pharmaceutical quality control.

I am a dedicated QC Biochemist with a strong background in medicinal chemistry and pharmaceutical science. My experience at TCoag has equipped me with the skills to perform routine QC analysis and manage product quality assessments in the field of Haemostasis and Haematology. I excel in writing reports, presenting findings, and moderating lab meetings, ensuring that all processes adhere to industry standards.

Throughout my career, I have demonstrated my ability to facilitate communication between R&D, manufacturing, and quality assurance teams, aligning product development with market needs. My commitment to continuous improvement is evident in my participation in Lean Six Sigma initiatives and my proactive approach to troubleshooting quality issues. I am passionate about improving patient outcomes through meticulous quality control and regulatory compliance.

Experience

Work history, roles, and key accomplishments

TC
Current

QC Biochemist

TCoag

Jul 2022 - Present (3 years 2 months)

Completed routine QC analysis and value assignments to assess suitability of in-vitro diagnostic products in Haemostasis and Haematology. Assisted in investigations related to product quality issues, wrote reports, and presented findings to the team. Coordinated Material Safety Data Sheets (MSDS) for finished products and carried out formulations for alternative sources and co-formulants.

AB

Quality Control Analyst

AbbVie

Oct 2021 - Jul 2022 (9 months)

Performed chemical analysis on finished drug substance, drug product, in-process materials, raw materials, intermediates, stability samples, and final APIs in accordance with cGMP. Supported other activities within the QC department, including analyzing samples relating to investigations, development, and stability. Reviewed, interpreted, and analyzed data for technical, quality, and compliance to

EM

Laboratory Technician

Enfer Medical

Jul 2021 - Oct 2021 (3 months)

Performed chemistry analysis of in-process/final product as per schedule and in accordance with regulatory requirements in a GMP environment. Authored documents ensuring cGMP compliance, such as laboratory investigations, deviations, and change controls. Maintained data integrity and ensured compliance with FDA, GLP, QSR, and cGMP regulations, as well as company SOPs and specifications.

Education

Degrees, certifications, and relevant coursework

Technological University Dublin logoTD

Technological University Dublin

B.Sc., Medicinal Chemistry and Pharmaceutical Science

Activities and societies: Student ambassador for the chemistry department; volunteered to organize a quiz competition for first-year students and participated in open days.

Studied Medicinal Chemistry and Pharmaceutical Science, gaining proficiency in various analytical instruments and techniques. Developed strong practical skills in laboratory procedures and chemical analysis.

Tech stack

Software and tools used professionally

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Tolu Oladimeji - QC Biochemist - TCoag | Himalayas