Manufacturing Process Engineer - Quality

As a Manufacturing Process Engineer - Quality, you will play a crucial role in analyzing and optimizing manufacturing and industrial processes with the aim of enhancing efficiency and reducing costs. Your responsibilities will include process designing, troubleshooting, optimization, analysis, documentation, quality control, project management, automation, and quality assurance. Collaboration with cross-functional teams, implementation of process improvement initiatives, and contributing to the overall success of the organization will also be key aspects of your role. Candidates with experience in the Quality department are preferred for this position. You will be tasked with conducting detailed evaluations and gap analyses to identify areas for improvement in existing manufacturing operations. Designing and implementing process optimization strategies to enhance efficiency, reduce cycle times, and improve product quality will be essential. Collaboration with Engineering, Production, and Quality teams to develop and maintain Standard Operating Procedures (SOPs) and Work Instructions will also be part of your responsibilities. Monitoring key process performance indicators such as cycle time, yield, scrap rate, and Overall Equipment Effectiveness (OEE) to meet or exceed operational targets will be crucial. Establishing and maintaining process control measures, including Statistical Process Control (SPC) techniques, to ensure consistent product quality and reduce variability will also fall under your purview. Providing technical troubleshooting support, leading process validation activities, participating in root cause analysis, corrective action, and preventive action (CAPA) initiatives, as well as delivering training to production teams on new processes and equipment will be part of your role. To qualify for this position, you should hold a Bachelor's degree in Mechanical, Plastics, Metallurgical, or Process Engineering and have 2-3 years of experience as a Process Engineer in a manufacturing environment, preferably in medical device or medical product manufacturing. Strong knowledge of process optimization, lean manufacturing, Six Sigma, and statistical analysis is required. Proficiency in process modeling, data analysis, SPC, and process simulation software is essential. Excellent problem-solving and analytical skills, along with the ability to manage complex process challenges, are also necessary. Additionally, you should have working knowledge of process safety, risk assessment, and regulatory compliance standards such as ISO 13485, ISO 14971, and FDA 21 CFR Part 820. Effective communication and interpersonal skills for cross-functional collaboration, strong project management abilities, and the capability to manage multiple priorities and deliver within deadlines are also important attributes for this role. If you are interested in this position, please contact Mr. Vigneshwaran S at 8925969558 from the HR & admin Team. This is a full-time, permanent position with benefits including food provision, health insurance, leave encashment, life insurance, and Provident Fund. The work location is in person, and the expected start date is 01/08/2025.,