senior regulatory affairs specialist in Singapore

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job details

life science
job type
working hours
3 years
reference number
adeline cheow, randstad
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job description

about the company

A multinational company with an outstanding reputation in providing full patient care solutions in a surgical room setting. The organisation prides themselves in providing high quality and innovative products to enhance clinical outcomes in the field of non-invasive therapeutic products, medical infrastructure and healthcare information technology solutions. The organisation is recruiting a Senior Regulatory Affairs Specialist to assist in the registration projects in Emerging Asia. This is a really exciting time to get on board!

About The Job

A fantastic opportunity for individuals who are skilled in Regulatory Affairs/ Quality Assurance. You would be actively involved in support the team for the product submission to the commercial partners.

As the Senior Regulatory Affairs Specialist of the organization, you are effectively required to:

  • Prepare and collect the regulatory documentations for submission to the Regulatory organization.
  • Support the RA team in the planning and implementation for license renewals, periodic updates, review labelling, obtain new registrations, review changes of existing products
  • Developing add reviewing documents such as dossiers, marketing material, advertisement and promotional literature.
  • Building effective relationships with key stakeholders and disseminate regulatory information to QA and R&D if there is any regulatory issue.

About The Manager/team

Reporting to the Regulatory Affairs Manager, you will be working closely with the regulatory affairs teams to achieve the organisation’s regulatory affairs functions.

Skills & Experience Required

To be successful in this role, you possess at least 3 years of working experience in Regulatory Affairs within the medical device or pharmaceuticals business.

To apply online please use the 'apply' function, alternatively you may contact Adeline at 65107401.
(EA: 94C3609/ R1765444 )


Product submission, prepare regulatory documentation


Understanding in Regulatory affairs is desired, experience in the medical devices is a bonus.


Senior Regulatory Affairs Specialist to assist in the registration projects in Emerging Asia.

educational requirements

Bachelor Degree