Job Description

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Your Tasks

• Key Responsibilities:
• Conduct audits in accordance to the relevant regulations, quality standards, policies, and other required criteria on the part of the auditor.
• Ensure timely completion of audit/surveillance and submission of audit report
• Develop and review audit methodologies for accreditation compliance
• Develop and conduct related training courses
• Provide support for other departments on day-to-day planning, marketing, operations, and new product development.
• Undergo relevant training, qualification, or certification process to be qualified to provide further services.
• To implement and uphold medical device laws and regulations of Malaysia
• To educate and train manufacturers at large on the importance of complying with the Malaysian Medical device laws and regulations
• To generate, compile and prepare assessment reports and recommendations for review of certification bodies.
• To plan, conduct and follow up on audits as assigned by the Head of the MHS Department i.e. MHS Manager to follow up on items assigned by Medical Device Certification bodies

Your Qualifications

• Key Requirements:
• Bachelor\'s degree in Electrical / Biomedical Engineering, Biomedical Science, Pharmaceutical, Chemical Engineering, Chemical Science, Biotechnology or relevant Sciences
• Have minimum 4 years of relevant experience in medical device manufacturing industry
• Have at least 2 years\' experience in Quality Management Systems (ISO 13485, MDD / MDR, MDSAPORorGDPMD)
• Clear and articulate presentation ability with excellent communication skills
• Travelling will be required

Additional Information

Required Experience:

Professionals 3 - 5 years of experience

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