Manufacturing Process Engineer
Covidien (St Louis, Missouri)
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Conducts technical projects either independently, as a team leader, or as part of a team to support manufacturing of terminally sterilized and aseptic manufactured products. The scope of these projects will include one or more of the following: 1) process modification to improve safety, product quality, yield and reduce costs, 2) the transfer of technology and processes from Research and Development to manufacturing, 3) equipment and process change control, commissioning and validation, 4) data trending on product performance characteristics for evaluating process control and solving product and process problems, 5) and conducting product and production Failure Investigations, implementing corrective actions, and preparing sound scientific reports. Highly motivated individual will take ownership of the process/product they support to provide guidance and upgrades to the manufacturing group. Requirements: Bachelor’s degree in Mechanical/Chemical Engineering or equivalent engineering degree. Three plus years of experience in a finished pharmaceutical or clinical diagnostics manufacturing environment, parenterals required. Three or more years of demonstrated knowledge of and experience in application of cGMP's, validation, quality systems, document control or manufacturing supervision. Must understand impact of regulatory considerations on engineering initiatives Knowledge of Six Sigma and Lean Manufacturing techniques required. Well-developed abilities with computers, process automation, and project management.
To apply online, please use the following link:Apply To Covidien