for Quality Engineer Key Responsibilities Assist in maintaining and updating QMS documentation SOPs Work Instructions Records Help coordinate internal audits and prepare documentation for external audits Support the training process by organizing sessions and maintaining training records Perform basic QC checks and inspections under supervision Assist with tracking and follow-up on CAPA actions Help maintain supplier documentation and support risk management files Ensure proper document control and record retention in compliance with ISO 13485 Promote awareness of quality procedures across departments Qualifications Experience Diploma or Bachelor s in Mechanical Engineering or related field 1-2 years of experience in a quality or manufacturing environment preferred Candidate must be from a medical Pharma background company with hands-on experience in ISO 13485 certification and compliance Familiarity with medical device regulations is an advantage Skills Required Basic understanding of QMS principles and ISO standards Good attention to detail and documentation accuracy Robust organizational and communication skills Proficient in Microsoft Office Word Excel Outlook Ability to follow procedures and work collaboratively in a team Job Type Full-time Job Types Full-time Permanent Pay Up to 40 000 00 per month