☑ Basic $ 4500 - $6500 + Transport Allowances $350 + AWS + Min 1.5 mth Variable Bonus
☑ 5 Days, 8.30am -5.30pm / 9.00am – 6.00pm
☑ Location: Central.
☑ MNC - Medical Device & Equipment Manufacturer
☑ Good Benefits & Career Prospect
Key Responsibilities:
- Ensure products and processes meet ISO standards and regulatory requirements.
- Lead internal and external audits and follow up on corrective actions.
- Manage the submission of regulatory documents for Singapore, Vietnam, and Thailand.
- Work closely with regulatory agencies to ensure compliance.
- Provide training on quality processes and support teams.
Requirements:
- Bachelor’s degree in Life Sciences, Pharmacy, Chemistry, or related field.
- 3-5 years of experience in QA and RA, ideally in medical devices.
- Knowledge of ISO 13485, ISO 9001, and local regulatory requirements.
- Strong attention to detail and good organizational skills.
Why Join Us? :
- Be part of a world leader in diagnostic imaging.
- Work in a friendly, supportive team with growth opportunities
Interested applicants are welcome to apply now or send your updated CV to [email protected]
Only shortlisted candidate will be notified
Yvette Kam Soo Leng
Registration: R22107492
