Marketing Chair

American Society for Quality (ASQ), Ottawa Valley Section, Ottawa, ON, Canada April 2026 - Present
  • Coordinate logistics and scheduling for workshops and networking events, facilitating continuous professional development for local quality and regulatory professionals in Ottawa.
  • Execute targeted promotional communications to drive society engagement.

R&D Intern

Engineering Department, Experimental Orthopedics Clinic, University Hospital Magdeburg, Germany May 2024 - Jun 2025
  • Spearheaded the development and implementation of an EU MDR (2017/745) compliant regulatory framework for the pre-market approval of an ongoing Class III hip and knee implant project.
  • Developed a project-specific QMS framework, streamlining traceability and cross-functional workflows between R&D, manufacturing, and compliance bodies for audit readiness.
  • Executed regulatory gap analysis across 21+ harmonized standards, validating the biological safety, mechanical endurance, and material properties of early-stage prototypes.
  • Formulated strategic action plans for development teams, effectively mitigating compliance risks and defining the roadmap for future product approval.

Biomedical Engineering Trainee

United Hospital Ltd., Dhaka, Bangladesh Dec 2017
  • Executed Quality Assurance (QA) protocols on Varian TrueBeam and Clinac Linear Accelerators, ensuring radiation safety compliance and operational accuracy.
  • Verified radiotherapy treatment simulations and planning using Varian Eclipse.
  • Supported the clinical execution of Brachytherapy, X-Ray, CT, and MRI procedures.
  • Validated the performance and safety of critical care systems, including ECGS, CTGs, patient monitors, and hospital medical gas infrastructure through quality checks and supply documentation.

Master's Thesis

Development and Application of a Regulatory Affairs Documentation System for University Research in the Field of Medical Devices.
  • Developed a general and project-specific market approval strategy for academia-developed medical devices to bridge the gap between research prototypes and regulatory compliance.
  • Structured an ISO 13485-aligned QMS streamlined for academia-led medical device design and development teams.
  • Designed a risk management system based on ISO 14971 containing implant-specific potential hazards, including FMEA and risk assessment.
  • Created a verification and validation plan ensuring valid scientific evidence for future conformity assessments.

Bachelor's Thesis

A Comparative Study of Imaging Modalities Used for Cancer Diagnosis.
  • Analyzed over 40 clinical CT, MRI, and PET/CT cases to compare spatial, contrast, and temporal resolution for cancer detection.
  • Compared the diagnostic capabilities of the above three imaging modalities to determine the best performance for lung, breast, brain, and metastatic cancer detection.
  • Produced cost, performance, and image-quality comparison to guide efficient modality selection in cancer diagnosis.

Strategic Regulatory Analysis of EU MDR vs. CMDR

Conducted a comparative analysis of the EU MDR and CMDR (SOR/98-282) framework to identify pre-market and post-market compliance distinctions. Evaluated structural QMS divergences, contrasting Canada's MDSAP and MDL/MDEL mandates against the EU's Notified Body conformity assessments. Demonstrated insights on approval timelines, clinical evaluations, and vigilance to guide global market-entry pathways.

Cost-Effective Dual-Function Foot Orthosis

Designed a dual-purpose orthotic sole to treat Bunion and Flat Foot. Developed a functional prototype and conducted user testing for design improvement. Validated biomechanical performance through gait analysis and optimized the design for cost-effectiveness.