Project Engineer

Major Duties and Responsibilities:

• Work with customers to understand project requirements and timelines, communicate concerns or questions about design or molding, provide customer with timely feedback on reaching project milestones, and exceed customer expectations with regard to service, cost, and delivery where reasonable.
• Work with external customers to develop quotes for new business opportunities.
• Work with Process Engineering and Toolmakers in the development of optimized injection-mold tooling for new or transfer products.
• Use customer-provided drawings or specifications, and consider Medbio quality requirements, to develop accurate and complete product specifications, purchased component specifications, assembly specifications, and bills of material for all new or transfer products.
• Work with Director of Engineering, Program Managers, and Process Engineer(s) to conceptualize, research, and implement new ideas, processes, and technologies for the betterment of Medbio Inc. and its customers.
• Write and execute comprehensive qualifications/validations for any processes that involve something other than non-standard molding.
• Train and/or provide guidance for Associate Project Engineers, as applicable.
• Work well with others in the organization to identify solutions and manage complex or difficult tasks
• Perform any other related duties as requested by the Program Manager
  
  

Organizational Relationships:

The Project Engineer reports to the Program Manager. This position works closely with other Project Engineers and/or Process Engineers, coordinates with Quality Assurance and Production on inspection or manufacturing activities, and provides project-specific information to Finance, Sales, and Operations as necessary

Experience and/or Educational Requirements:

• Engineering or relevant degree or equivalent in experience.
• (Prefer) 2-3 years experience in plastic injection molding.
• Good understanding of automation systems and equipment.
• Strong computer skills (Microsoft Office, MS Project).
• Strong product and tool ‘blueprint’ reading skills.
• Strong written/verbal communication skills.
• Good understanding of ISO and FDA regulations and GMPs.
  
  

Physical Requirements:

Must be able to work and perform what would be considered standard practices for this type of positions in the industry.