Adrien Mopoho
Montreal,Canada
Summary
Emerging biotechnology professional with strong foundations in GMP‑regulated environments, QA documentation systems, biologics workflows, and analytical laboratory methods. My experience spans radiopharmaceutical manufacturing, softgel product development, and preclinical assay research. I am pursuing the Biopharmaceutical & Diagnostics stream of the IMI‑MBioTech program to develop advanced expertise in biomanufacturing operations, quality systems, regulatory compliance, and biotech product development.
Overview
2
2
years of professional experience
Work History
Quality Assurance Associate (Internship)
Jubilant Radiopharma
05.2023 - 09.2023
- Ensured GMP audit readiness by organizing and maintaining controlled QA documentation, batch records, and regulatory files.
- Conducted preliminary batch record reviews, identified documentation gaps, and verified compliance with SOPs and regulatory standards.
- Prepared materials for internal audits and regulatory inspections, supporting traceability and data integrity.
- Improved documentation retrieval efficiency by 30% through redesign of document organization and indexing systems.
- Supported QMS tasks including controlled document updates, change management, and alignment with compliance guidelines.
Product Development Intern – R&D
Capcium
09.2022 - 12.2022
- Drafted and revised Master Batch Records (MBRs) and Standard Operating Procedures (SOPs) for GMP-compliant softgel manufacturing.
- Collaborated with QA, QC, and R&D teams to ensure accuracy, regulatory alignment, and cross-department documentation consistency.
- Analyzed API specifications and technical data to support formulation and production documentation integrity.
- Compiled raw material and production data supporting cost estimation, supply planning, and operational decision-making.
- Standardized document formatting structures, decreasing MBR discrepancies and improving production workflow efficiency.
Research Assistant – Chemical Sciences
NuChem Sciences
09.2021 - 12.2021
- Conducted compound synthesis, solution prep, and fluorescence-based biochemical assays for preclinical drug development.
- Implemented analytical techniques and quantitative assay workflows, ensuring accurate data collection and interpretation.
- Maintained high-quality laboratory records in line with GLP and data integrity principles.
- Assisted in optimization of assay protocols and early-stage screening approaches.
Education
Bachelor of Science - Biology
Concordia University
Montreal, Canada05.2025
Skills
- GMP/QA Compliance: Batch record review, controlled documentation, internal audits, CAPA support, deviation tracking, QMS documentation
- Regulatory Documentation: SOP/MBR authoring, document lifecycle management, FDA & Health Canada expectations, traceability, risk-based assessment
- Analytical & Lab Techniques: Fluorescence assays, spectrophotometry, compound prep, exposure to LC‑MS/MS, HPLC/UPLC, biochemical assay design
- Software & Systems: MS Office, Excel data analysis, EDMS/DMS systems, regulatory tracking tools
Regulatory & Quality Competencies
- GMP/GLP/GCP compliance; QMS documentation
- SOP/MBR development; document lifecycle control
- CAPA methodology; deviation & root-cause investigation
- FDA / Health Canada regulatory expectations
- Biosafety & risk assessment (CL1, CL2, CL3 exposure)
Professional Strengths
- Strong communication and cross‑functional collaboration (QA, QC, R&D)
- High attention to detail in regulated settings
- Process‑driven thinking and analytical problem solving
- Adaptability in fast‑paced biotech environments
- Technical writing & documentation accuracy
Languages
English
Native or Bilingual
French
Professional Working
Timeline
Quality Assurance Associate (Internship)
Jubilant Radiopharma
05.2023 - 09.2023
Product Development Intern – R&D
Capcium
09.2022 - 12.2022
Research Assistant – Chemical Sciences
NuChem Sciences
09.2021 - 12.2021
Bachelor of Science - Biology
Concordia University