Description
Manage the APQP process for new programs.
Trains production personnel and works with Process Engineering to transfer new programs to production.
Interacts with customers and other technical personnel to assist with the development and design of the product and processes to improve functionality and manufacturability.
Identify and select equipment and technologies to be used for new products and processes.
Develops preventative maintenance plans.
Conducts FMEA, DOE, SPC analysis and uses other quality tools to fulfill customer requirements and manufacturing initiatives.
GD & T. Interpret and apply geometric dimensioning and tolerancing.
Provides technical guidance and direction for manufacturing.
Participates in research and development activities in terms of process implementation and validation of processes / products, process improvement and metrics.
Provides input for new product equipment selection, installation and maintenance.
Writes detailed `work instruction-level documents for manufacturing operations and related areas. Summarily trains personnel in these instructions and other technical process controls.
Conducts engineering studies and analyzes data.
Maps work flow(s) and develops process control plans.
Directs the validation activities for new tools, processes and equipment.
Develops and submits validation packages for customer approval of new parts, design modifications and / or process changes.
Develops and evaluates inspection methods and measurement capabilities.
Evaluates process stability and capability.



Requirements
Skills/Qualifications:

Bachelor's degree (B. S.) in engineering with Three years' related experience in manufacturing environment ( medical device experience preferred).

CONTACT:
Chad Crow
ccrow@jobscss.com
610-771-1086