Manufacturing jobs in Singapore

Job summary

An innovative MedTech firm in Singapore is seeking a Regulatory & Quality Specialist responsible for ensuring compliance with ISO 13485 and FDA regulations across global manufacturing sites. This role entails governance of the Quality Management System and oversight of audits and inspections while requiring strong communication and risk-based decision-making skills. Candidates should hold a relevant bachelor's degree and have 3-5 years of experience in medical device quality or regulatory affairs. Competitive salary and benefits offered.

Benefits

Qualifications

• 3-5+ years of experience in medical device Quality and/or Regulatory Affairs.
• Strong knowledge of manufacturing quality systems and audits.
• Experience driving compliance within manufacturing environments.

Responsibilities

• Act as the central QA/RA authority for internal manufacturing sites worldwide.
• Maintain and govern the global ISO 13485-compliant QMS.
• Lead internal audits and support FDA inspections.