Raqa Specialist

**Your new company**
Join one of the leading medical device company today Excellent opportunities for learning RAQA work

**Your new role**
- **Perform IVD Product registration (Class A to D) with HSA in time and in accordance with the global product launch schedule and local launch plan.**
***:

- **Effective operate regulatory pathway for medical devices in SEA region (Singapore, Malaysia, Thailand, Indonesia and others)**
***:

- **Communicate and align with the global regulatory team to get support for local product registration and manage local regulatory systems and processes.**
***:

- **Manage a post-market surveillance i.e. CAPA, FSCA, Recall, and Customer complaints.**
***:

- **Prepare and respond to quality audits conducted by the global and notified body.**

***

**What you'll need to succeed**
- At least 2 years of relevant regulatory affairs experience in IVD / Medical Device industry
- Min. Bachelor’s degree holder in Life Sciences / Pharmacy
- Relevant experiences in regulatory affairs or a similar role/function

**What you'll get in return**
You will be part of a leading organization who values employees and have a structured career growth with development opportunities. You will also be compensated with attractive remunerations.

**What you need to do now**

Registration ID No. R1330566 EA License No.: 07C3924 Company Registration No: 200609504D #1241681