Manufacturing Process Specialist

1 month ago

Monument, Colorado, United States Jabil Full time
  • Job Overview
  • SUMMARY: Responsible for delivering direct engineering assistance to the production lines within the manufacturing sector. Ensures adherence to process specifications and product qualifications.
  • Key Responsibilities:
  • Employs Lean and Six Sigma principles along with analytical problem-solving techniques to identify and execute engineering projects aimed at resolving manufacturing challenges, minimizing costs, reducing waste, enhancing quality, and shortening cycle times.
  • Provides technical guidance and leadership for daily manufacturing activities, ensuring that key performance indicators such as Production, Quality, Scrap, and Cycle Time are achieved.
  • Identifies opportunities and formulates action plans to enhance process reliability and equipment uptime.
  • Offers engineering support for product inquiry investigations.
  • Conducts comprehensive assignments that encompass entire projects or segments of significant projects.
  • Determines appropriate methods and techniques or modifies standard practices to accommodate variations.
  • Coordinates efforts with external vendors.
  • Establishes manufacturing capabilities to facilitate intra-company product transfers.
  • Delivers technical expertise to support special initiatives, pilot operations, product and process enhancements, risk management strategies, and contributes to the development of capital expenditure forecasts and equipment/spare parts budgets to meet business requirements.
  • Assists in supplier evaluations for services/products as necessary.
  • Ensures compliance with safety protocols and procedures, including responsibilities related to the Environmental Management System.
  • Adheres to Records Management Policies, Records Retention Schedules, company Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records, and third-party vendor protocols if applicable.
  • Additional responsibilities may be assigned, and not all duties listed may be allocated.
  • Implements effective corrective actions to address quality, safety, and ergonomic risks identified in the manufacturing environment.
  • Management & Supervisory Duties:
  • May oversee activities and supervise the completion of tasks assigned to other personnel.
  • Qualifications:
  • Experience in the medical device sector, including knowledge of Good Manufacturing Practices (GMP).
  • Familiarity with product and process design and development, materials, standardization, and applied statistics.
  • Proficient in word processing, spreadsheet analysis, data management, project management, presentation graphics, engineering analysis, and statistical software such as MiniTab.
  • Knowledge of information systems, including but not limited to Enterprise Resource Planning (ERP), Quality Systems, and Documentation Control Systems like Windchill.
  • Project management and cost analysis knowledge preferred.
  • Education and Experience:
  • Bachelor's or Master's degree in Engineering.
  • Three to five years of experience in a medical device environment.
  • Advanced technical training in Finishing is preferred.

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