Quality Manager

Job Description: 1. Oversee all stages of production—including sheet metal forming, CNC machining, and weldment assembly—to ensure consistent quality and adherence to customer specifications and tolerances. 2. Lead the development and execution of inspection plans, including first article inspections (FAI), in-process checks, and final product validation, using advanced metrology tools and techniques. 3. Ensure all products meet industry-specific regulatory requirements, such as FDA guidelines for medical devices, automotive production part approval processes (PPAP), and semiconductor cleanroom standards. 4. Conduct periodic internal audits to assess QMS compliance, identify non-conformities, and implement corrective and preventive actions. 5. Identify opportunities for process optimization, waste reduction, and defect prevention using data-driven methods like root cause analysis, statistical process control (SPC), and corrective action planning. 6. Act as the primary point of contact for quality-related customer inquiries, audits, and feedback, ensuring timely resolution of issues and maintaining strong relationships with clients in the medical, automotive, and semiconductor sectors. 7. Oversee the development, implementation, and maintenance of the Quality Management System (QMS) to ensure compliance with relevant standards and regulations. 8. Producing statistical reports on quality standards and reporting to the Management team and Managing director 9. Drive root cause analysis and corrective action processes. Qualifications: • Bachelor’s degree in Engineering (Mechanical, Industrial, or related field), Quality Management, or a comparable technical discipline. • Minimum of 7 years of experience in quality management within a manufacturing environment, preferably in sheet metal fabrication, machining, or weldment production serving medical, automotive, or semiconductor industries. • Proven expertise in interpreting technical drawings, geometric dimensioning and tolerancing (GD&T), and industry-specific quality standards (e.g., ISO 9001, ISO 13485, AS9100, IATF 16949). • Experience conducting Gauge Repeatability and Reproducibility (GR&R) studies to validate measurement systems and ensure inspection accuracy. • Familiarity with quality management systems (QMS) and continuous improvement methodologies such as Lean, Six Sigma, or Kaizen. • Strong understanding of regulatory and compliance requirements specific to the medical (e.g., FDA), automotive (e.g., PPAP, APQP), and semiconductor industries. • Experience in lean medical or continuous improvement is a plus. • Strong analytical skills and attention to detail, with the ability to identify and resolve technical issues effectively. • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams. • Knowledge of statistical analysis techniques and quality control methodologies, such as Six Sigma, Lean Manufacturing, or Statistical Process Control (SPC), is advantage.