No more applications are being accepted for this job
- Location: Metropolis Buona Vista
- Salary: $6,500 per month
- Duration: June 1st, 2024 – May 31st, 2025 (with potential extension based on performance review and approval)
- Major Job Scope:Support AA Dermal Fillers Lifecycle Management (80%)
Other Therapy Area Devices related tasks (20%) - Medical device background with at least 5 years of experience
- Experience with China/Japan registration or support roles
- Clinical trial experience
- Proficiency in handling both active and non-active medical devices:Active medical devices (requiring power/electricity)
Non-active medical devices (e.g., syringes) - Manage and support AA Dermal Fillers throughout their lifecycle
- Undertake tasks related to other Therapy Area Devices
- Contribute to regulatory activities and submissions
- Collaborate with cross-functional teams to ensure compliance with regulations and standards
- Assist in preparing for and participating in audits and inspections
- Stay updated with regulatory changes and industry trends
Regulatory Specialist - Singapore - RECRUIT EXPRESS PTE LTD
Description
Roles & ResponsibilitiesExciting Opportunity: Sr. RA Specialist (Medical Devices) at Pharma MNC - Metropolis Buona Vista
We are seeking a talented Sr. RA Specialist to join our team at a leading pharmaceutical multinational corporation (MNC) in Metropolis Buona Vista
Job Details:
Mandatory Qualification:
Nice-to-Have Qualifications:
Responsibilities:
How to Apply:
If you meet the qualifications and are eager to take on this challenging role, please send your resume and cover letter to We are excited to welcome a dedicated Sr. RA Specialist to our team at this prestigious pharmaceutical MNC in Metropolis Buona Vista
Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)
Company EA Licence number : 99C4599
Personnel EA License: R1331820
Biochemistry
Drug Development
Cell
Microsoft Excel
Regulatory Compliance
Legislation
Healthcare
Fillers
Chemistry
Compliance
Medical Devices
Audits
Regulatory Submissions
Manufacturing
Audit