Dhebi Adam

Recent Regulatory Affairs graduate with a strong academic foundation in health sciences, human kinetics, and psychology.

I am interested in beginning my career in Regulatory Affairs, Quality Assurance, Compliance, or related life sciences roles where I can apply my scientific background, research skills, attention to detail, and understanding of regulatory requirements.

Combining regulatory education with a strong scientific foundation.

I am a recent Regulatory Affairs graduate from Humber Polytechnic with a Bachelor of Science in Human Kinetics and a minor in Psychology.

My academic background has given me experience working with scientific information, research, evidence-based analysis, technical concepts, and detailed documentation.

Throughout my Regulatory Affairs education, I developed an understanding of regulatory processes, compliance, documentation, product requirements, and the role regulatory professionals play in helping health-related products meet applicable standards.

I am currently seeking an entry-level opportunity where I can continue developing my regulatory knowledge while contributing strong organization, analytical thinking, communication, and attention to detail.

Academic Background

POSTGRADUATE EDUCATION

Regulatory Affairs

Humber Polytechnic

Focused on the regulatory environment surrounding healthcare and life science products, including regulatory documentation, compliance, product requirements, and regulatory processes.

UNDERGRADUATE EDUCATION

Bachelor of Science in Human Kinetics

Minor in Psychology

Developed a strong foundation in human health, physiology, scientific research, critical analysis, and evidence-based thinking, complemented by the study of human behaviour and psychology.

Regulatory, Scientific & Professional Skills

Academic training in Regulatory Affairs, combined with a strong scientific background and transferable professional skills.

REGULATORY KNOWLEDGE

Regulatory Affairs

  • Health Canada regulatory environment
  • Food and Drugs Act and related regulations
  • Medical device regulatory concepts
  • Drug and natural health product frameworks
  • Regulatory documentation and submission awareness
  • Labelling, compliance, and quality-related concepts

SCIENTIFIC & ANALYTICAL

Research & Analysis

  • Scientific literature review
  • Evidence-based analysis
  • Research interpretation
  • Human health and physiology knowledge
  • Critical thinking and problem solving
  • Data interpretation and synthesis

PROFESSIONAL SKILLS

Communication & Organization

  • Technical and professional writing
  • Attention to detail
  • Organization and document management
  • Clear written communication
  • Collaboration and teamwork
  • Managing deadlines and priorities

Regulatory Affairs Projects

Selected academic projects demonstrating the practical application of regulatory research, documentation, compliance, scientific analysis, and lifecycle planning.

01

Regulatory Submission

Developed components of a simulated pharmaceutical regulatory submission involving quality and scientific documentation, clinical evidence, stability, risk management, pharmacovigilance, and benefit-risk assessment.

Regulatory Documentation • Scientific Review • Risk Management

02

Product Labelling Analysis

Evaluated healthcare product labels against Canadian regulatory requirements for drugs, medical devices, natural health products, and cosmetics.

Labelling • Compliance Review • Regulatory Research

03

Regulatory Change Plan

Designed a regulatory workflow for product lifecycle changes including shelf-life extension, label updates, DIN discontinuation, Health Canada review, and post-market monitoring.

Regulatory Strategy • Change Control • Lifecycle Management

What I Bring

Scientific foundation
Regulatory education
Analytical thinking
Attention to detail
Written and verbal communication

Let's connect.

I am interested in opportunities where I can begin my career in Regulatory Affairs and contribute my scientific and analytical background.