Quality Assurance Manager Job Hiring in Saudi Arabia for Nhara Healthcare Industries

Career Opportunity in Saudi Arabia!

Job Vacancy: Quality Assurance Manager
Employer/Company: Nhara For Manufacturing Company / Nhara Healthcare Industries
DMW Registration / Accreditation No.: 10457884
Job Location: Saudi Arabia

Quality Assurance Manager

Qualifications:

• Minimum of 5 years work experience
• Proven experience in a managerial or supervisory role, 3-5 years, overseeing QA teams and processes.
• Knowledge of QMS, experience conducting internal and external audits, Compliance with local and international regulatory standards.
• Extensive experience with regulatory requirements, such as ISO 13485, and other relevant standards and regulations.
• Several years (5-10) of experience in the medical device industry, particularly in quality

Requirements:

• Detailed RESUME
• Certificate of Employment
• Candidate must have ready passport

☑ NO TRADETEST FEES,
☑ NO MEDICAL FEES,
☑ NO PLACEMENT FEE,
☑ NO PROCESSING FEE,
☑ NO SALARY DEDUCTION,
💯% NO FEES TO BE COLLECTED

Please report to our office for preliminary interview.
Please bring 2 copies of your CV/ Resumes and supporting documents (COE, trainings, seminars), bring original for verification. Business Hours: Mon – Fri: 9:00 AM – 6:00 PM

International Skill Development, Inc.
Address: ISD Building, 5439 Curie Street Palanan, Makati City, Philippines

Employer Overview:

Nhara is a medical manufacturing company, established to manufacture high end medical products in Saudi Arabia, export them to global markets, and improve the efficiency of the health sector locally.

FOR MANPOWER POOLING ONLY.
NO FEES in any form and/or purpose will be collected from the applicants.
Beware of illegal recruiters and human traffickers.
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Quality Assurance Manager Job Hiring in Saudi Arabia for Nhara Healthcare Industries

Qualifications:

Minimum of 5 years work experience
Proven experience in a managerial or supervisory role, 3-5 years, overseeing QA teams and processes.
Knowledge of QMS, experience conducting internal and external audits, Compliance with local and international regulatory standards.
Extensive experience with regulatory requirements, such as ISO 13485, and other relevant standards and regulations.
Several years (5-10) of experience in the medical device industry, particularly in quality”,
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