درباره من
As a seasoned professional in standardization and documentation, I specialize in ensuring compliance with industry standards. Proficient in developing and implementing standardized processes, particularly in medical engineering and quality management. Expertise includes guiding organizations through ISO 13485, ISO 9001, MDR, and post-market compliance. Adept at creating comprehensive documentation systems that meet regulatory requirements, fostering efficiency and quality assurance in all aspects of the business
Quality Assurance
Providing documents for product registration in Yemen, Egypt, Libya, and Sri Lanka.- Registering UDI-DI in EUDAMED.- Closing non-conformities after audits and CAPA closure.- Providing documentation for audits.- Handling registration in the Obelis platform and submitting documents to obtain certificates.- Preparing self-declarations for some Class IIa and Class I produ
MODE · 1403 - 1402
SALES REPRESENTATIVE
•Engagement with prospective and existing clients to understand their needs and provide tailored solutions.
•Demonstrate excellent communication skills through the creation and delivery of compelling sales pitches,
persuasive emails, and effective follow-up calls.
•Build strong relationships with clients to foster long-term partnerships and ensure customer satisfaction.
•Identify and pursue new business opportunities, contributing to the expansion of the customer base.
•Skillfully negotiate terms, prices, and contracts to achieve mutually beneficial agreements with clients.
•Prepare accurate and detailed proforma invoices, ensuring clarity and transparency in all financial transactions.
•Collaborate with internal teams, such as marketing and customer support, to enhance overall customer
experience and address client needs.
•Demonstrate a track record of achieving and exceeding sales targets.
•Utilize relevant sales tools, ERP systems, Social Media, Advertising.
TEKNOMED · 1402 - 1401
MEDICAL DEVICES QUALITY CONSULTANT
•Implemented and developed ISO 13485 and MDR
•Created technical documentation for medical devices
•Implemented ISO 14971 for risk management
•Conducted regulatory affairs and internal auditing
•Sourced raw materials for factories
•Registered medical equipment and laboratory kits with the Ministry of Health
•Facilitated audits by notifying the relevant bodies
•Assessed the quality of medical and laboratory product
Freelancer · 1401 - 1397
Quality management
The university located in Istanbul, Turkey
İstanbul Kültür Üniversitesi · 1400–1402
Biomedical Engineer
The University located in Mashhad in Iran
Azad University · 1396–1400
ISO 9001 Auditor AND MDR
ISO 9001 Auditor AND MDR
IQC · 1
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سفارش سرویس
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پاسخدهی
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پروژه در جریان
مدتها پیش
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اطلاعات تماس
موبایل
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