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    • You should have at least 1 year of regulatory experience in medical devices and a related science degree.
    • Partnering with a global Medical Device MNC with an…
    • Support the development of resources and delivery of trainings for internal medical and non-medical functions.
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    • The Associate Executive supports the day‑to‑day operations of Medical Affairs, particularly the Clinical Governance team.
    • Contribute to improving clinical governance and medical affairs operations.
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    • This role is also responsible for medical governance oversight for the department.
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    • Experience with sterile products, combination products, or Class II/III medical devices .
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    • Support medical and quality related work.
    • Draft responses to medical enquires and complaints.
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    • Working knowledge of applicable medical device regulations and guidelines.
    • Good understanding of medical terminology and basic human anatomy.
    • Review and assess local and overseas medical and non-medical claims within policy terms and conditions and claims authority limit within stipulated turnaround…

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Job Post Details

Regulatory Affairs & Quality Assurance Executive [Medical Device / Up to 5,500] - job post

INTEGRITY PARTNERS PTE. LTD.
Singapore
$4,000 - $5,500 a month - Permanent
You must create an Indeed account before continuing to the company website to apply

Job details

Pay

  • $4,000 - $5,500 a month

Job type

  • Permanent

Location

Singapore

Full job description

  • Regulatory Affairs & Quality Assurance Executive with global Medical Device MNC
    • Opportunity to work on local and regional submissions


Partnering with a global Medical Device MNC with an established branding, our client is seeking a Regulatory Affairs & Quality Assurance Executive .


Reporting to the RA Director, we are looking for someone with good knowledge of regulatory framework.

In this role, you shall assist in the execution of the regulatory strategies in assigned markets throughout the company product life cycle, with a focus on efficient pre-market and post- market regulatory approvals.

You will also support the review and approval of:

  • Change control activities
  • Product promotional activities
  • Product registration
  • Product labeling
  • Regulatory inspections and audits

You should have at least 1 year of regulatory experience in medical devices and a related science degree.


For more information, please apply with your updated CV (in Word document).


Ambrose Chan
Registration Number: R1218177
EA License Number: 17C8502

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