Job Details:
-Performs the daily visual, clean, and verification checks as defined by departmental procedures and batch record instructions
-Manufacturing of components and finished medical device products
-Compiling documentation for builds and storing
-Following GMP and ensure the cleanroom and production areas are maintained and meet the required standards of cleanliness
-Experience using microscopes
-Monitoring the manufacturing process at different stages & reporting results to Engineering department
-Manufacturing of devices for validation and verification purposes
-Prepares samples and records for the R&D department
-Calibrating and carrying out preventative maintenance on equipment
-Training new personnel on the manufacture of products
-Working with internal customers to resolve quality issues
-Reviewing current work practices to identify areas in which quality could be improved
-Assist QA Document Control with document & record administration as needed
-Balloon bonding experience
-Previously worked in a FDA regulated environment
-Previously worked within a cleanroom environment

EXPERIENCE & SKILLS:
-The role requires a person with 2 – 4+ years’ experience in catheter assembly and sub assembly processes
-The person needs to enjoy working individually and also as part of a team, in a varied role with a broad scope
-Previous experience of working a lean manufacturing environment and demonstrated problem solving ability is an advantage

Job Apply Expiry Date: Jun 03, 2015
Apply Email Address: caroline.dowling@collinsmcnicholas.ie
Contact #: 917006706
Company Name: tbd