Our client is seeking a Contract Regulatory Affairs Specialist (2 Months Contract) to provide support for medical device registration across the Asia-Pacific region. Based in Singapore, this role involves preparing regulatory submissions to health authorities, supporting local partners, maintaining compliance records, and ensuring licenses are current and accurate. You will also provide key regulatory support to internal teams including Sales, Operations, and R&D.
Key Responsibilities
- Prepare, compile, and format documents for regulatory submissions.
- Maintain and update regulatory trackers and databases (e.g., license status, expiry dates).
- Organize and archive regulatory files, approvals, and correspondence.
- Prepare standard forms, letters, and certificates for local partners and distributors.
- Track submission timelines and follow up with agents/distributors for required documents.
- Provide valid licenses and certificates to internal teams as needed.
- Generate simple status reports and PowerPoint updates on submissions and approvals.
- Coordinate meetings with local partners and health authorities.
- Bachelor’s degree in Engineering or Life Sciences (other fields may be considered).
- At least 1 year of experience in Regulatory Affairs, Quality Assurance, or another regulated environment.
- Strong interest in regulatory affairs and compliance.
- Excellent attention to detail with the ability to manage multiple priorities.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Strong written and verbal communication skills in English; additional language skills are an advantage.
Please note: Due to the anticipated high volume of applications, only shortlisted candidates will be contacted. All information provided will be treated with strict confidentiality and used solely for recruitment purposes.
Cheah Wei Ee
Principal Consultant - Retail & Hospitality Division
EA Personnel No: R23114782
Peoplebank Singapore Pte Ltd | EA Licence No: 08C5248