Process Engineer

at  Ambu

A GLOBAL JOB POSITION WITH AN IMPACT:

We are growing and expanding our Manufacturing Site in Mexico! In the job as Process Engineer, you will have the opportunity to actively support the organization by meeting ensuring that our manufacturing site runs as needed to have the growth expected of the products we make in Mexico, excel in your own daily tasks and responsibilities, and experience a very varied working day in a dynamic.
The Process Engineer to provide engineering support for testing, production-pilot, transfer, installation, validation, start up, stabilization and documentation of new products and equipment integration into manufacturing sites.

EDUCATION AND EXPERIENCE:

• An Associates of Industrial Engineering, Mechanical, Manufacturing, or similar or

  equivalent combination of education and experience.

• 1-3 years of experience or equivalent knowledge and skills to perform the position

  responsibilities.

• Experience in the medical device industry or medical field

DUTIES/RESPONSIBILITIES:

• Assess shop capacity and make recommendations to increase capacity to meet

  business demands.

• Identify & implement shop floor process improvements that increase output and

  reduce overall costs.

• Assist MFG team in developing new product validation program and assure

  compliance to reduce the launch time.

• Perform walkthroughs, inspections, product evaluation and testing as needed.

• Conduct Engineering test evaluations such are: GR&R, SVs, Test Method, Criticality.

• Ability to understand and utilize assembly documentation such as but not limited to

  the following: Schematics, BOM’s, Visuals, Debug, Testing tools and procedures.

• Provide clear direction and training for production associates.

• Advise on scheduling and staffing needs.
• Provides guidance, training, and leadership to new technicians or clerks.

• Responsible for ensuring personal and Company compliance with all Federal, State,

  local and Company regulations, policies, and procedures.

• Demonstrated success in working across functions, organizations, and all levels of

  management.

• Achieving results through other team members and suppliers. Drive for action and

  quality focused.

• Must be a highly motivated, proactive, self-directed worker.

• Knowledge of NPI Process/Development (preferred)

• Ability to read, analyze, and interpret general new product/manufacturing/quality

  procedures or medical regulations.

• Ability to write Completion Reports or Engineering Studies, and procedure manuals.

• Ability to interpret an extensive variety of technical instructions in mathematical or

  diagram form and deal with several abstract and concrete variables.

• Ability to interpret and manipulate various types of testing and CAD data.

• Ability to write test and interpret CAD data.

responsibilities.

• Experience in the medical device industry or medical fiel