Intern - Quality Assurance & Regulatory Compliance
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Before you apply
LocationSri Lanka
Work modeon-site
Typeinternship
SeniorityEntry
DepartmentQuality Assurance & Regulatory Compliance
Company size10,000+ people
First seenOct 18, 2026 · 2w ago
Verified live15h ago
At a glanceSummarised by Seekless from the posting.
Undergraduate or recent graduate in Biomedical Engineering, Electronics Engineering, Life Sciences, or a related field
Strong attention to detail and analytical thinking skills
Good communication and documentation skills
Ability to work independently as well as collaboratively within a team
Support and conduct comprehensive product and system testing in line with design verification plans
Troubleshoot test results, identify root causes, and recommend corrective actions
Analyze test data to ensure compliance with defined acceptance criteria and regulatory standards
Prepare detailed reports on test outcomes, known issues, deviations, and proposed solutions
Support regulatory documentation activities for medical devices, including technical files and submissions
Assist with quality system activities aligned with ISO 13485 requirements
Collaborate cross-functionally with engineering, product, and clinical teams to support product development and compliance activities
Basic understanding of medical devices or healthcare regulations is an advantage
Exposure to ISO 13485 or quality systems is a plus
Intern - Quality Assurance & Regulatory Compliance
About the company
Twinery - Innovations by MAS is a core pillar at MAS. We develop scientific and engineering solutions that transform the human/textile interface, putting groundbreaking, life-improving technologies right next to your skin. Our innovations transform businesses, enhance lives and reshape expectations. We are on the lookout for a passionate and dedicated individual to fill this role within our Wave Tech team.
Key Responsibilities:
•
Support and conduct comprehensive product and system testing in line with design verification plans.
•
Troubleshoot test results, identify root causes, and recommend corrective actions.
•
Analyze test data to ensure compliance with defined acceptance criteria and regulatory standards.
•
Prepare detailed reports on test outcomes, known issues, deviations, and proposed solutions.
•
Support regulatory documentation activities for medical devices, including technical files and submissions.
•
Assist with quality system activities aligned with ISO 13485 requirements.
•
Collaborate cross-functionally with engineering, product, and clinical teams to support product development and compliance activities.
Qualifications:
•
Undergraduate or recent graduate in Biomedical Engineering, Electronics Engineering, Life Sciences, or a related field.
•
Basic understanding of medical devices or healthcare regulations is an advantage.
•
Exposure to ISO 13485 or quality systems is a plus.
•
Strong attention to detail and analytical thinking skills.
•
Good communication and documentation skills.
•
Ability to work independently as well as collaboratively within a team.
Location - Twinery, Colombo, Foster Lane.