Our client is in Scientific and Medical industry. Due to their current expansion plan, they are looking for a RA Specialist to join their Regulatory, in hopes of developing the current high performing team. They are located in the Central area – easily accessible.
Duties of RA Specialist:
- Ensure compliance with regulatory standards for medical devices and biotechnology products, preparing and submitting necessary documentation.
- Assist in product registration, renewal, and change submissions, liaising with regulatory agencies and suppliers.
- Develop regulatory strategies and provide guidance during product development for timely market access.
- Maintain accurate regulatory documentation and records for submissions and approvals.
- Support Quality Assurance to ensure regulatory compliance and participate in audits when needed.
- Collaborate with internal teams to integrate regulatory requirements into product launches and provide regulatory training.
- Identify regulatory risks and develop mitigation strategies for product marketing and commercialization.
- Monitor post-market safety data, reporting adverse events as required by authorities.
Requirements:
- Degree in Life Science or related field
- Relevant 3 to 5 years experience in handling regulatory affairs for similar industry
Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.
We regret that only shortlisted candidate will be notified
- Email Address: [email protected]
- EA License No: 19C9682
- EA Personnel No: R2199158
- EA Personnel Name: Soo Wei De
