Regulatory and Quality Assistant

Full-Time | Night Shift | Remote

PH-Based Applicants Only

We're looking for a Regulatory and Quality Assistant to support quality management systems, regulatory compliance activities, and product documentation while ensuring adherence to international medical device standards.

What We're Looking For:

• Previous experience working in a regulatory, quality assurance, or ISO-certified environment (required)

• Minimum of 2 years of relevant experience in Regulatory Affairs or Quality Assurance

• Medical Device industry experience is required

• Strong understanding of ISO 13485, MDSAP, CE Marking, FDA requirements, or similar regulatory frameworks

• College Degree or relevant certification in Regulatory Affairs, Quality Management, or related fields preferred

• Excellent written and verbal English communication skills

• Strong attention to detail and documentation accuracy

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)

• Excellent organizational, analytical, and problem-solving skills

• Ability to manage multiple priorities and work independently

• Positive attitude, strong work ethic, and willingness to learn and grow

Why Join Us

• Fully remote work setup

• Full-time, stable opportunity with an international team

• Work within the highly regulated and growing medical device industry

• Gain exposure to global quality and regulatory standards

• Collaborative and supportive work environment

• Opportunity for continuous professional development and career growth