Industrial Engineer
HR Works
- Arroyo, PR
- Permanente
- Tiempo completo
- Conduct comprehensive time studies on manufacturing processes to identify bottlenecks, reduce waste, and increase efficiency.
- Design, test, and implement lean manufacturing techniques to optimize production flow and minimize production time.
- Collaborate with cross-functional teams, including production, quality assurance, and supply chain, to develop and implement process improvements.
- Utilize statistical analysis and industrial engineering tools to analyze production data, predict production issues, and devise strategic solutions.
- Develop and maintain detailed documentation of process changes, time study results, and efficiency improvements for internal and regulatory compliance.
- Train and guide production staff on new processes and techniques resulting from time study analysis and optimization efforts.
- Continuously monitor and evaluate production processes, making recommendations for further improvements and innovations.
- Participate in the design and implementation of new production lines, ensuring optimal layout and efficiency from the start.
- Lead root cause analysis for production issues and develop corrective action plans to prevent recurrence.
- Stay informed on the latest industry trends, technologies, and best practices in industrial engineering and time management.
- Bachelor's degree in Industrial Engineering or a closely related field.
- 3-4 years of hands-on experience in industrial engineering within a medical device manufacturing environment.
- Proven track record of conducting time studies and implementing process improvements in a manufacturing setting.
- Strong knowledge of lean manufacturing principles and Six Sigma methodologies.
- Proficient in the use of industrial engineering software and tools for statistical analysis, process simulation, and time study analysis.
- Excellent problem-solving, analytical, and organizational skills.
- Ability to work effectively in a team environment and communicate complex ideas clearly and concisely.
- Self-motivated with the capability to manage multiple projects under tight deadlines.
- Knowledge of FDA regulations and ISO standards related to medical device manufacturing is highly desirable.