Key Responsibilities - Maintain review and update QMS documentation SOPs Work Instructions Records to ensure accuracy and compliance - Lead coordination of internal audits and prepare comprehensive documentation for external audits - Support and sometimes lead training sessions maintaining and updating training records - Conduct detailed QC checks and inspections independently ensuring adherence to quality standards - Track analyze and follow-up on CAPA actions driving timely closur - Manage supplier documentation and contribute to supplier quality management and risk assessment activities - Ensure robust document control and record retention in strict compliance with ISO 13485 - Promote and enforce awareness of quality procedures across departments offering guidance to junior team members Qualifications Experience - Diploma or Bachelor s in Mechanical Engineering or related field - 4- 5 years of experience in a quality or manufacturing workplace preferred - Strong knowledge of ISO 13485 and medical device regulations is an advantage Skills Required - Solid understanding of QMS principles and ISO standards - Excellent attention to detail and ability to maintain documentation accuracy - Strong organizational analytical and communication skills - Proficient in Microsoft Office Word Excel Outlook - Ability to work independently take ownership of tasks and collaborate effectively within a team