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Epicareer might not working properly because your browser javascript is turned off.

What is JavaScript?

JavaScript is like the magic behind making websites interactive. Basically, it makes Epicareer more enjoyable and engaging.
How do i turn this on?
Find tutorial for your browser below :
  1. Make sure the webpage is open.
  2. In the Safari app on your Mac, choose Safari > Preferences, then click Security.
  3. Make sure the Enable JavaScript checkbox is selected.
  4. Click Websites.
  5. On the left, click Content Blockers.
  6. Make sure Off is chosen in the pop-up menu next to the website.
  7. On the left, click Pop-up Windows.
  8. Make sure Allow is chosen in the pop-up menu next to the website.
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  1. Open Chrome on your computer.
  2. Click. then Settings.
  3. Click Privacy and Security.
  4. Click Site settings.
  5. Click JavaScript.
  6. Select Sites can use Javascript.
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  1. If you're running Windows OS, in the Firefox window, click Tools > Options.
  2. Tip: If you're running Mac OS, click the Firefox drop-down list > Preferences.
  3. On the Content tab, click the Enable JavaScript check box.
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  1. Click the "Settings and more" icon at the top right of the Edge browser window.
  2. Click Settings.
  3. From the Settings menu, click Cookies and site permissions.
  4. Scroll down and click on JavaScript.
  5. In the JavaScript window, toggle the slider to "on" or "allowed."
  6. Close the Settings tab.
  7. Refresh the page.
Visit Site here
  1. Go to Settings.
  2. Click Advanced in the left sidebar, and click Privacy & security.
  3. Under Privacy and security, click Site settings.
  4. Click JavaScript.
  5. At the top, turn on or off Allowed (recommended).
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Jobs or company...

Quality Director(AWS|ISO 13485)

RM 23,000 - RM 23,000 / month
Checking job availability...
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Job Scope:

The Quality Director will lead and oversee all quality assurance, compliance, and continuous improvement initiatives to ensure the highest product quality, regulatory compliance, and customer satisfaction. This role is responsible for developing and implementing strategic quality objectives, enhancing operational efficiency, and maintaining compliance with global medical device regulations and industry standards.

Key Responsibilities:

  • Develop, implement, and maintain the Quality Management System (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, MDR (EU), MDSAP, and other relevant regulatory requirements.
  • Ensure adherence to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
  • Lead internal and external audits and manage relationships with regulatory bodies, ensuring successful certifications and approvals.
  • Oversee supplier quality management, including supplier audits, qualification, and performance monitoring.
  • Drive quality improvement initiatives, including Six Sigma, Lean Manufacturing, and Root Cause Analysis (RCA) methodologies.
  • Monitor Key Performance Indicators (KPIs) related to product quality, defects, and non-conformances, ensuring corrective and preventive actions (CAPA) are effectively implemented.
  • Champion a Zero Defect Culture, ensuring process standardization and optimization to reduce waste and inefficiencies.
  • Lead and mentor a team of Quality Engineers, Quality Assurance (QA) Managers, and Inspectors, fostering a culture of accountability and excellence.
  • Collaborate with R&D, Engineering, Manufacturing, and Supply Chain teams to integrate quality into every stage of product development and production.
  • Provide training and awareness programs on quality standards, regulatory requirements, and best practices.
  • Address customer complaints, warranty issues, and field failures, ensuring timely investigations and resolution.
  • Act as the primary point of contact for regulatory authorities, notified bodies, and external auditors.
  • Develop and present quality performance reports to senior leadership, driving informed decision-making.

Job Requirements:

  • Bachelor’s or Master’s degree in Engineering, Quality Management, or a related field.
  • Minimum 10-15 years of experience in quality management, preferably in a medical device, electronics manufacturing environment.
  • Strong understanding of ISO 13485, FDA regulations, MDR, and other medical device standards.

Job Type: Full-time

Pay: Up to RM23,000.00 per month

Schedule:

  • Monday to Friday

Supplemental Pay:

  • 13th month salary
  • Performance bonus

Work Location: In person

Expected Start Date: 03/31/2025