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Please Turn on your JavaScript

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...

Regional Regulatory Affairs Manager (Medical Device)

Salary undisclosed

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Partnering with a global Medical Device MNC with an established branding, our client is seeking a Regional Regulatory Affairs Manager to join their team in Singapore.

Responsibilities

  • Responsible for regulatory activities across Southeast Asia - regulatory submissions, compliance for new or existing products
  • Support ANZ RA team on regulatory related activities for their region
  • Manage registration plans for new products, variations, modifications, registration renewals
  • Analyse registration complexity and provide regulatory advice to internal groups to support company’s business objectives
  • Collect and analyse regulatory intelligence, and incorporate regulatory trends into decision-making processes
  • Approval of product labelling with local regulations
  • Maintain awareness of regulatory requirements or changes
  • Provide post market regulatory support and guidance as required
  • Follow up on product license renewal
  • Any other ad-hoc duties as assigned

Requirements

  • Degree in Life Sciences, Engineering, or related discipline
  • At least 5 year of related working experience, preferably in the medical device industry
  • Possess good knowledge of regulations and requirements for medical devices, GDPMDS (Good Distribution Practice for Medical Devices), EU Medical Device Directive/ Regulation, US FDA guidance, ISO standards (13485, 9001)
  • Knowledge and specialization in Regulatory and Quality Affairs (Quality Control/Assurance) is an advantage
  • Excellent communication skills and English at work proficiency level (writing and conversational)
  • Proficient in Microsoft Office
  • Independent, meticulous, detail-oriented, and proactive
  • Ability to Multi-task & Proactive
  • Positive working attitude with passion to learn and develop
  • Able to adapt in a fast-paced environment
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