Engineer II, Product

The Engineer II, Product is responsible for supporting product improvements through adherence to established design control processes, good engineering and documentation practices. The key responsibility of this position is to complete intermediate projects with guidance from more experienced engineers and managers. They will gain exposure to some of the complex tasks, exercise judgement and take action while adhering to defined procedures during project support & improvements.

Occasionally the Engineer II will be directed in several aspects of the work on the more complex tasks.

• Immediate expectations
• Conducts independent analysis and develops solutions to problems
• Develops approaches and designs where precedent usually exists
• Performs developmental and/or test work that relies heavily on a comprehensive knowledge of theory and design
• Support initiatives for continuous process and product improvements
• Writes detailed design specifications
• Receive general project direction and solicits input from more experienced engineers while supporting project timelines and milestones, and bring them to completion on time and within budget
• Completion of CAPA tasks and deliverables (Corrective and Preventive)
• Work on special projects as they arise
• Long term expectations
• Initiate and manage projects with adherence to program management guidelines
• Coordinate efforts with the Materials Group to assess vendors and provide materials technical information
• Build productive relationships internally and externally
• Assists in training new/current employees with respect to documentation, use of equipment, laboratory techniques and department procedures
• Delivers communications tailored to the needs of the receiver (managers, peers, customers) with appropriate frequency to maximize its utility and promote cross-functional collaboration.

• Competent in your domain. Familiar with other areas of domain expertise within the team
  • Understanding of strength of materials, automation, plastic injection molding, part assembly, fixturing, testing, and process control techniques
  • Solid works to interpret part dimensions, sectional views, conduct mates, build assemblies
  • Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.) - use of Minitab Software for analysis
• Knowledge of the Medical Device Industry and familiarity with FDA QSR Regulations is a plus
• Has a basic understanding of best practices. Has a basic to intermediate understanding of engineering discipline
• Have awareness of the broader product strategy and contribute to it
• Ability to receive general project direction and solicit input from more experienced engineers
• Requires the ability to independently make decisions that impact the attainment of project objectives

• Must be at least 18 years of age
• Bachelor's degree from an accredited college or university (Engineering or Technology)
• 2-4 years' experience

• This is largely a sedentary role.
• This job operates in a professional office environment and routinely uses standard office equipment.
• Work may be performed in a clean room environment
• While performing the duties of this job, the employee may be required to sit or stand for long periods of time; depending on the machine they are operating
• Must be able to occasionally move and lift objects of up to 25 lbs
• Typically requires travel less than 5% of the time