Process Engineer I

• Impactful Work: When you join Diasorin you become part of a team thats dedicated to improving lives. Your contributions will directly impact patient care making a meaningful difference in the world.

• Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world expanding your horizons and contributing to global healthcare solutions at the forefront of the diagnostic industry.

Job Scope

The Process Engineer Iwill be responsible for identifying opportunities and implementing changes to improve manufacturing processes add efficiencies reduce costs implement tooling and production equipment assembly methods quality standards and material flow.
The Process Engineer I will assist with Instrument Manufacturing processes associated with Instrument Manufacturing Production Quality Control and Depot.

Key Duties and Responsibilities

• Participates in or leads major process improvement initiatives from identification to execution
• Identifies gaps in processes develops project plans and cost reduction/avoidance. Monitors progress and assess adequacy of output/deliverables
• Champions the understanding and application of Lean principles and techniques to maximize yield capacity and capability
• Creates and maintains Manufacturing Instructions routings and associated processes. Ensures effective training for new or changed processes
• Manages/Executes process validation activities for IQ (installation qualification) OQ (Operational Qualification) and PQ (Performance Qualification)
• Analyzes and maintains Value Stream Maps for ongoing processes to ensure efficient factory utilization
• Participates in infrastructure optimization and expansion
• Utilizes Lean methodology (e.g. DMAIC Lean Manufacturing Continuous Improvement (Kaizen) PDCA etc.) to support the design of optimal processes
• Designs and implements layout of equipment materials and work cells for maximum efficiency
• Analyzes factory data and recommends projects activities to improve overall factory efficiency
• Analyzes manufacturing and field defect data and creates and implements process improvement programs.
• Deploys standard processes and communicates cross-functional needs
• Develops best practices and standardized operating instructions to optimize processes
• Evaluates processes and equipment to ensure compliance with applicable environmental safety and quality regulations and standards
• Monitors and reduces process variation using techniques such as Statistical Process Control (SPC) Root-Cause Analysis Data Analytics Scripting Database Query Development Product Flow Optimizations and Tableau Dashboard Development
• Participates in the development and maintenance of FMEAs and Control Plans
• Eliminates human errors by utilizing Poka Yoke
• Utilizes Line balancing cycle time and take time to ensure customer requirements are met
• Creates ROI justifications to support process improvement initiatives
• Leads Design of Experiments (DOE) on existing and upcoming processes
• Interfaces directly with assemblers leads and production supervisors in resolving production problems
• Identifies automation opportunities and implements solutions
• Ability to complete hands-on tasks up to and including actual equipment production runs
• Monitors procedural and engineering change releases; assess departmental impact
• Analyzes develops processs and implements Engineering Change Orders (ECO) Manufacturer and Departmental Document change control (MCO & DCO)
• Ensures effective departmental interfaces; facilitates interdepartmental communication
• Escalates problems and potential issues through management channels as necessary
• Additional task and duties as assigned

Education Experience and Qualifications

• Bachelors Degree Industrial Manufacturing or Mechanical Engineering or related technical field with required relevant work experience. required
• 2 Years Process engineering or manufacturing experience in relevant industry with educational requirement preferred
• 2 Years Years Process engineering or manufacturing experience in relevant industry with advanced degree requirement preferred
• 1 Years Years Experience in a GMP and FDA regulated industry and/or a ISO certified organization preferred
• Proficient in Microsoft Word Excel Access Visio and PowerPoint programs. (High proficiency)
• Thorough knowledge of cGMP regulations (High proficiency)
• Highly organized with proven time management and prioritization skills. (High proficiency)
• Ability to work independently (High proficiency)
• Ability to handle tight deadlines frequent assignment changes periodic heavy workload rapidly changing technology and dynamic business growth (High proficiency)
• Strong statistical and data analysis skills; knowledge of Statistical Process Control (SPC) and Design of Experiment (DOE) (High proficiency)
• Ability to use a systematic approach for Root Cause Analysis and knowledge of systems/processes to ensure data-driven decisions (High proficiency)
• Ability to handle multiple projects and lead positive change (High proficiency)
• Experience with time study methodologies and industrial engineering basics (High proficiency)
• Team player capable of working across functional groups to qualify new processes/ materials under a compressed schedule (High proficiency)
• Experience with LEAN Manufacturing and Six Sigma Problem solving Methodology (High proficiency)
• Ability to effectively solve complex technical problems (Medium proficiency)
• Develop in-depth knowledge across multiple business units and technical areas (Medium proficiency)
• Excellent interpersonal and oral and written communication skills (Medium proficiency)
• Mechanical design capabilities utilizing Solidworks is preferred (Medium proficiency)
• Lean Six Sigma Black Belt preferred
• ASQ Certified Quality Engineer. preferred

Whatweoffer

Receive a competitive salary and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world.