Sr OPEX Engineer
Job Summary:
We are seeking a highly skilled and experienced Senior Operational Excellence (OPEX) Engineer to join our team in the medical device manufacturing sector. The ideal candidate will have a strong background in Continuous Improvement (CI) methodologies, Six Sigma, and Root Cause Analysis (RCA) to drive Safety, Quality, Delivery, and Cost (SQDC) objectives. This role is critical in ensuring our manufacturing processes are efficient, effective, and compliant with industry standards.
Key Responsibilities:
- Lead and manage Continuous Improvement (CI) projects to enhance operational efficiency and effectiveness.
- Utilize Six Sigma methodologies to identify, analyze, and solve complex manufacturing problems.
- Conduct Root Cause Analysis (RCA) to identify underlying issues and implement corrective actions.
- Develop and implement strategies to achieve Safety, Quality, Delivery, and Cost (SQDC) objectives.
- Collaborate with cross-functional teams to drive process improvements and ensure alignment with business goals.
- Monitor and analyze key performance indicators (KPIs) to track progress and identify areas for improvement.
- Provide training and mentorship to team members on CI, Six Sigma, and RCA methodologies.
- Ensure compliance with regulatory requirements and industry standards in all operational activities.
- Prepare and present reports on project status, performance metrics, and improvement initiatives to senior management.
Qualifications:
- Bachelor's degree in Engineering, Operations Management, or a related field. Advanced degree preferred.
- Minimum of 7 years of experience in operational excellence, continuous improvement, or a related role in the medical device manufacturing industry.
- Certified Six Sigma Black Belt or equivalent certification.
- Proven track record of leading successful CI projects and achieving measurable improvements.
- Strong analytical and problem-solving skills with the ability to conduct detailed RCA.
- Excellent communication and interpersonal skills with the ability to work effectively in a team environment.
- Knowledge of regulatory requirements and industry standards in medical device manufacturing.
- Proficiency in data analysis tools and software (e.g., Minitab, JMP, Excel).
