About this role
Responsible for managing daily regulatory affairs operations and submissions to ensure compliance within the South-East Asia market. This includes handling change assessments, monitoring regulatory updates, and supporting product safety alerts and audits.
Requires a degree in Engineering or Science, with 1-2 years of medical device regulatory experience preferred. Fresh graduates are also encouraged to apply.
What they're looking for
Regulatory AffairsRegulatory SubmissionsComplianceTechnical WritingChange AssessmentProduct LabelingRegulatory IntelligencePost Market Surveillance
Frequently asked questions
What does a Associate Regulatory Affairs Specialist SEA at Arthrex do?
Responsible for managing daily regulatory affairs operations and submissions to ensure compliance within the South-East Asia market. This includes handling change assessments, monitoring regulatory updates, and supporting product safety alerts and audits. Requires a degree in Engineering or Science,…
What skills does this Associate Regulatory Affairs Specialist SEA role need?
Key skills for this role include Regulatory Affairs, Regulatory Submissions, Compliance, Technical Writing, Change Assessment, Product Labeling.
How much does a Associate Regulatory Affairs Specialist SEA at Arthrex pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Associate Regulatory Affairs Specialist SEA role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Associate Regulatory Affairs Specialist SEA role?
You can apply directly on Arthrex's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.