Paul K.

Key Skills

Software

Other

Label Studio

Top Subject Matter

Pharmaceutical quality control and GMP compliance

Pharmaceutical operations

QA documentation

Top Data Types

Document

Text

Audio

Top Task Types

Classification

Data Collection

Question Answering

Text Summarization

Text Generation

Transcription

Evaluation/Rating

Function Calling

Prompt + Response Writing (SFT)

Fine-tuning

Freelancer Overview

Quality Control / Quality Assurance Intern (Cosmos Pharmaceutical Ltd). Brings 3+ years of professional experience across complex professional workflows, research, and quality-focused execution. Core strengths include Other. Education includes Bachelor of Technology, Technical University of Kenya (2024). AI-training focus includes data types such as Document and Text and labeling workflows including Classification and Data Collection.

Labeling Experience

Customer Service & Order Management Assistant (Mission for Essential Drugs and Supplies)

OtherTextData Collection

Worked in order management for a pharmaceutical organization by validating and processing high-volume pharmaceutical orders with compliance-oriented record keeping. Coordinated with warehouse and logistics teams while maintaining QA-aligned documentation and resolving order discrepancies. Supported inventory tracking to improve stock accuracy and operational control through structured data management. • Processed and validated order information for accuracy and compliance. • Maintained audit-ready documentation and records aligned with QA requirements. • Resolved discrepancies with customers to ensure correct order fulfillment. • Supported inventory tracking through structured record updates.

2025 - 2026

Quality Control / Quality Assurance Intern (Cosmos Pharmaceutical Ltd)

OtherDocumentClassification

Served as a Quality Control/Quality Assurance intern performing routine laboratory testing and documenting results to support product compliance. Captured and recorded laboratory data with accuracy and traceability to maintain audit-ready quality records. Assisted with GMP- and regulatory-aligned documentation processes used for compliance review. • Recorded laboratory test outcomes and maintained traceable documentation. • Supported QA processes following GMP and regulatory requirements. • Assisted audit preparation by organizing and contributing to documentation. • Analyzed and reported laboratory data for quality oversight.

2024 - 2024

Education

Work History