Skip to main content
Upload your CV and find your next job on Indeed!

Medical Device Regulatory jobs

Sort by: -
    • You should have at least 1 year of regulatory experience in medical devices and a related science degree.
    • In this role, you shall assist in the execution of the…
    • Conduct periodic environmental scanning of the medical device market to prepare for appropriate regulatory controls for novel innovative medical devices.
  • View similar jobs with this employer
    • Assist in updating and maintaining laboratory SOPs, and preparation of documentations for ethics submissions, audits and regulatory inspections.
    • Vii. Provide training, competency assessment, and supervision of junior medical technologists, medical technologists, and phlebotomists (where applicable).
    • This role requires a compliance expert to lead & support global environmental regulatory strategies for our consumer electronic products.
    • Assist medical technologist to maintain adequate inventory of the unit’s supplies and materials.
    • Maintain a record of all repairs and routine maintenance of the…
    • Understanding of regulatory framework for medical devices is preferred.
    • Execute pre-market activities required to support the entire lifecycle of a medical…
    • 1–3 years of experience in Quality Control Microbiology or Environmental Monitoring in a GMP-regulated environment (pharmaceutical, biologics, or medical device…
    • Support regulatory submissions with biocompatibility sections (Technical Files, Design Dossiers, CERs) and maintain product compliance, technical files, and…
    • Preferably 3 to 5 years of relevant experiences in biopharmaceutical and/or medical device manufacturing industry and prior technical knowledge in batch…
    • The Specialist, Commercial Quality & Regulatory Affairs will prepare regulatory submissions and interact with regulatory agencies/health authorities to obtain…
    • Our literature review and synthesis projects involve the identification of clinical, economic and real-world evidence to support the value of a pharmaceutical…
    • Minimum 5 + years of experience in Regulatory Affairs or a regulated medical device environment, with exposure to manufacturing , distribution or regulatory…
    • We are seeking a detail-oriented Quality Engineer with experience in the medical device or healthcare products industry to ensure compliance with regulatory…

People also searched:

mbbs

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

Let Employers Find YouUpload Your Resume