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Vincent Nyakubaya

@vincentnyakubaya

Message

Quality control chemist specializing in GMP-compliant analytical testing and process improvement.

Zimbabwe

Message

What I'm looking for

I seek roles where I can apply GMP/ICH expertise to improve analytical methods, strengthen QMS, lead process improvements, and ensure compliant, timely product release.

I am a quality control expert with over five years of experience verifying product safety in GMP laboratories across pharmaceutical, mining, and government sectors.

I specialize in chromatographic and spectrometric techniques (HPLC, CE, LC-MS, ICP-OES, FAAS, ELISA) and have a strong record of method development, validation, and regulatory compliance to FDA/ICH/USP/BP standards.

I have driven process improvements through root cause analysis, CAPA management, SOP optimization, and QMS innovation, and I launched a QMS platform to enhance compliance and traceability for regulated industries.

I am known for precision, teamwork, and delivering timely, accurate results while maintaining rigorous documentation and safety-focused laboratory practices.

Experience

Work history, roles, and key accomplishments

Current

Co-Founder

Current

Radqal (Private) Limited

Sep 2024 - Present (1 year 1 month)

Launched Cleanite, an eco-conscious surface cleaner brand, and spearheaded Radqal Systems, a QMS platform to enhance compliance and traceability for regulated industries.

Product Launch & Compliance Traceability entrepreneurship Regulatory Strategy

Operations Manager

Laureate Le International Beauty Academy

Mar 2023 - Dec 2023 (9 months)

Streamlined workflows and improved documentation practices to align operations with quality standards and enhance operational efficiency.

Operations Management Process Improvement Documentation SOPs Team Coordination

Senior Associate, Quality Control

Amgen via 3-Key Consulting Inc.

Nov 2017 - Oct 2020 (2 years 11 months)

Reviewed and approved chromatographic datasets (HPLC, CE) for biologics ensuring FDA/ICH compliance; conducted stability testing for injectables with 100% on-time delivery of drug release studies and reduced data discrepancies through process improvements.

Stability Testing FDA Compliance CAPA LIMS

Graduate Assistant

West Virginia University

Aug 2010 - May 2017 (6 years 9 months)

Developed and validated a capillary electrophoresis method for steroid analysis in zebrafish plasma and reviewed datasets for endocrine disruption studies to ensure regulatory and protocol alignment.

Method Development Validation OECD Guidelines Matlab Analytical Chemistry

Laboratory Analyst

Global Platinum Resources

Dec 2009 - Jul 2010 (7 months)

Performed fire assay and ICP-OES analyses for platinum group metals in mineral ores, ensuring accurate assay results for mining operations.

FaaS Analytical Chemistry

Quality Control Chemist

Pharmanova

May 2009 - Nov 2009 (6 months)

Validated HPLC methods for generic tablets and syrups under ICH/USP/BP guidelines and authored QC reports, addressing analytical outliers to meet batch release specifications.

USP)QC Reporting SOPs