About this role
Quality & Regulatory Affairs Consultant at UL Solutions. Location: Kuala Lumpur, Kuala Lumpur, Malaysia. Role: preparing submissions, conducting research, reviewing documentation Requirements: Bachelors preferred (medical/engineering/science), 2+ years QA or regulatory affairs experience in medical devices, proficiency with Microsoft Office, strong written/verbal English and communication, attention to detail and multitasking. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Office Commitment: Full Time Workplace: Onsite Languages: English