Summary
Overview
Work History
Education
Skills
Websites
Projects
Certification
Timeline
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TABARAK SHAIKH

Toronto,Canada

Summary

Driven and meticulous professional with an MSc in Medical Device Regulatory Affairs, keen to leverage expertise and enthusiasm for regulatory compliance within the healthcare industry. Eager to apply academic background and practical experience to enhance regulatory processes and promote patient safety.

Overview

7
7
years of professional experience
1
1
Certification

Work History

Regulatory Affairs Intern

Purcell Global
04.2024 - 06.2024
  • Classified devices by Health Canada's medical devices classification rules and designed pre-clinical and clinical trial frameworks that align with Canadian regulations, incorporating innovative methodologies for efficiently evaluating respiratory disease management technologies
  • Produced comprehensive plans for pre-clinical and clinical trial phases, including timelines, milestones, and critical considerations for success in the Canadian market
  • Developed patient recruitment and data management strategies to ensure compliance with Canada's privacy laws and ethical standards
  • Effectively managed comprehensive document management processes, ensuring regulatory compliance and document accuracy.
  • Facilitated communication between the company and Health Canada

Executive

IFEDORA SERVICES PRIVATE LIMITED
09.2019 - 08.2022
  • Submitted and processed Inpatient, outpatient, and procedure insurance claims after verification according to the criteria of different insurance within the TFL
  • Reviewed patient accounts and collaborated with the medical providers to ensure billing and document policies
  • Coordinated with heads of different departments for various billing issues
  • Have done qualitative and quantitative audits
  • Worked with different medical software.

Service Engineering Intern

AUSSIN INTENSIVE CARE PVT. LTD
06.2017 - 09.2017
  • Helped regularly calibrate medical devices to ensure they provide accurate readings and outputs
  • Conducted routine checks and scheduled maintenance on medical equipment
  • Assisted in the installation and setup of new medical equipment, ensuring it was correctly configured and operational
  • Conducted tests to verify that newly installed or repaired equipment meets manufacturer specifications and regulatory standards
  • Helped maintain accurate records of maintenance activities, repairs, and service calls, including completing service reports and updating equipment logs.

Education

MASTER OF SCIENCE IN REGULATORY AFFAIRS -

Northeastern University
Toronto, Canada
06.2024

BACHELOR OF ENGINEERING IN BIO-MEDICAL -

Gujarat Technological University
Gujarat, India
05.2018

DIPLOMA OF ENGINEERING IN BIO-MEDICAL -

Gujarat Technological University
Gujarat, India
06.2015

Skills

  • Canadian Medical Devices Regulations and Guidelines
  • FDA Medical Devices Regulations and Guidelines
  • GMP Knowledge
  • Document Management and Preparation
  • Medical Device Establishment License (MDEL), Medical Device License (MDL), 510(k) and PMA application
  • ISO 13485 and ISO 14971
  • Strong attention to detail
  • Analytical thinking
  • Strong organizational capability
  • Ability to work independently with minimal supervision
  • Excellent verbal and written communication skills
  • Microsoft Excel and Microsoft Word

Projects

  • Developed comprehensive applications for Medical Device Establishment Licenses (MDEL) and Medical Device Licenses (MDL) for Class III and IV devices, including all requisite supporting documentation.
  • Formulated regulatory strategies for Class II and III devices, encompassing 510(k) and PMA submissions with detailed safety and effectiveness data.
  • Prepared and submitted an electronic Common Technical Document (eCTD) for a pharmaceutical product, ensuring strict adherence to regulatory guidelines.
  • Developed a comprehensive Quality Management System (QMS) manual adhering to the regulations of 21 CFR Part 820, ISO 13485, and ISO 14971 for Class I and II devices


Certification

ISO 13485:2016 Medical Device Lead
Auditor

Timeline

Regulatory Affairs Intern

Purcell Global
04.2024 - 06.2024

Executive

IFEDORA SERVICES PRIVATE LIMITED
09.2019 - 08.2022

Service Engineering Intern

AUSSIN INTENSIVE CARE PVT. LTD
06.2017 - 09.2017

MASTER OF SCIENCE IN REGULATORY AFFAIRS -

Northeastern University

BACHELOR OF ENGINEERING IN BIO-MEDICAL -

Gujarat Technological University

DIPLOMA OF ENGINEERING IN BIO-MEDICAL -

Gujarat Technological University
TABARAK SHAIKH