We are looking for a skilled Quality Assurance Engineer with hands-on experience in regulated industries to support quality systems, compliance, and continuous improvement initiatives. Key Responsibilities: Manage and support Quality Management Systems (QMS), Lead CAPA, non-conformance, and root cause investigations, Conduct internal audits and ensure compliance with FDA, ISO (9001/13485), and GMP standards, Support validation activities (IQ/OQ/PQ) and documentation, Collaborate with cross-functional teams to improve product and process quality. Requirements: Bachelor's degree in Engineering, Life Sciences, or related field, 3-6 years of Quality Assurance experience (Medical Device / Pharma preferred), Strong knowledge of ISO 13485, FDA regulations, and GMP, Experience with CAPA, audits, validation, and documentation, Good analytical, problem-solving, and communication skills. Employment Type: Contract. Only W2 no C2C.