Yusuf Adeniran
Mississauga,ON
Summary
Quality and GMP professional with a strong background in regulated manufacturing and quality systems in pharmaceutical production. Proven track record in quality documentation review, deviation investigations, and CAPA management, supporting a robust quality culture and continuous improvement in high-compliance operations.
Overview
6
6
years of professional experience
Work History
Process Technician – GMP Manufacturing
Eurofins CDMO Alphora
Oakville, Canada
06.2025 - Current
- Support manufacturing operations in a highly regulated GMP production environment ensuring adherence to quality standards and regulatory requirements.
- Review batch production records, logbooks and controlled documentation to maintain compliance with established quality management systems.
- Collaborated with Quality Assurance, Quality Control, and production teams to ensure operational compliance and foster quality culture in manufacturing operations.
- Supported investigations of quality events, including deviations, and assisted in documenting corrective and preventive actions to enhance compliance.
- Maintain documentation accuracy and traceability supporting internal audits and regulatory inspections.
- Contributed to consistent manufacturing quality standards by adhering to GMP procedures and implementing quality system controls.
Pharmacist
Upviews Pharmacy and Stores Ltd
, Nigeria
12.2022 - 03.2025
- Ensured compliance with pharmaceutical regulatory standards for medication storage, handling, and dispensing, safeguarding patient safety.
- Achieved accurate documentation and traceability of pharmaceutical products and inventory, enhancing operational integrity.
- Facilitated quality monitoring processes, including adverse reaction reporting and safety documentation, improving patient care and regulatory adherence.
Production Pharmacist
AKOL Pharmaceuticals
, Nigeria
12.2021 - 11.2022
- Executed pharmaceutical production and packaging processes in accordance with Good Manufacturing Practice standards to ensure product quality.
- Documented production data and maintained accurate records to enhance quality system traceability.
- Followed manufacturing procedures and established protocols to ensure adherence to quality compliance.
Intern Pharmacist
Oyo State Hospital Management Board
, Nigeria
08.2020 - 09.2021
- Monitored medication safety and maintained regulatory documentation to ensure compliance.
- Documented adverse drug reactions to enhance patient safety initiatives.
- Assisted pharmacists in preparing and dispensing medications to patients.
- Conducted medication reviews to ensure safety and efficacy for patients.
- Provided patient counseling on medication usage and side effects.
Education
Postgraduate Diploma - Quality Assurance and Regulatory Affairs
Academy of Applied Pharmaceutical Sciences
Toronto06-2026
Bachelor of Pharmacy -
Olabisi Onabanjo University
NigeriaSkills
- GMP programs
- Quality management systems
- Quality documentation systems
- Root cause analysis
- Documentation control
- Internal audit readiness
- Supplier quality awareness
- Food safety culture
- Continuous improvement
- Excel data tracking
- Microsoft Office proficiency
- Cross-functional collaboration
- Training support
Websites
Languages
- Yoruba
- English, Fluent
- Yoruba, Native
Quality And Regulatory Knowledge
- Good Manufacturing Practices
- Quality Management Systems
- Deviation Investigation and CAPA
- Documentation Control
- Root Cause Analysis
- Regulatory Compliance
Timeline
Process Technician – GMP Manufacturing
Eurofins CDMO Alphora
06.2025 - Current
Pharmacist
Upviews Pharmacy and Stores Ltd
12.2022 - 03.2025
Production Pharmacist
AKOL Pharmaceuticals
12.2021 - 11.2022
Intern Pharmacist
Oyo State Hospital Management Board
08.2020 - 09.2021
Postgraduate Diploma - Quality Assurance and Regulatory Affairs
Academy of Applied Pharmaceutical Sciences
Bachelor of Pharmacy -
Olabisi Onabanjo University