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zakir_canada

Zakir H.

@zakir_canada
5,0(1)

Regulatory Affairs Specialist

Pakistan
Engels
Sommige informatie wordt in het Engels weergegeven.
Over mij
I’m Zakir, a MedTech Regulatory Specialist and ISO Lead Auditor with 10+ years of experience. Based in Canada, I specialize in EU MDR (2017/745) and IVDR compliance for Class I through Class III medical devices. I help manufacturers navigate the complex path to CE Marking by delivering audit-ready Technical Files (STED), CERs, Risk Management (ISO 14971), and PMS/PMCF documentation. My unique perspective as an auditor ensures your documentation is structured to pass Notified Body reviews with zero friction. Let’s secure your market clearance.... Lees meer

Skills

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zakir_canada
Zakir H.
offline • 
Gemiddelde reactietijd: 1 uur

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Technische teksten
I will provide eu mdr 2017 technical documentation
5,0(1)
Regelgeving voor medische hulpmiddelen
I will build an iso 13485 qmsr quality management system for the medical device

Portfolio

Werkervaring

Freelance Regulatory Documentation Specialist

Independent Consultant

May 2024 - Feb 20259 mos

Delivered freelance regulatory documentation services for startups and SMEs. Developed technical documentation, risk management reports, and clinical documentation in line with EU MDR and ISO standards. Focused on clear, structured, and compliant regulatory deliverables.

Regulatory Affairs Specialist

Medical Device Regulatory Consultancy

Mar 2023 - Feb 202411 mos

Provided regulatory consulting and documentation support for medical device manufacturers. Assisted in EU MDR transition projects, documentation remediation, and alignment with harmonised standards. Collaborated with cross-functional teams to ensure audit-ready submissions.

Regulatory Affairs Specialist

Pharma Consultancy

Jan 2020 - Apr 20222 yrs 3 mos

Worked on EU MDR (2017/745)–compliant technical documentation for Class I–III medical devices. Prepared and reviewed Technical Files, Design Dossiers, CERs, Risk Management files (ISO 14971), PMS/PMCF plans, IFUs, and labeling. Supported regulatory gap analyses and conformity assessment readiness for EU market access.

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Specificering van de beoordeling
  • Communicatieniveau van de freelancer
    5
  • Kwaliteit van de levering
    5
  • Waarde van de levering
    5
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    zevsek

    SI

    Slovenië

    5

    Very professional service provider. He delivered technical documentation that exceeded my expectations. I will definitely hire him again.

    US$ 400-US$ 600

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    6 dagen

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    Technische teksten

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