Process Engineer Pharmaceuticals Aseptic

Process Engineer
St. Louis, MO
This individual will conduct technical projects either independently, as a team leader, or as a 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 and/or reduce costs,
2) transfer of processes from Research and Development to manufacturing,
3) equipment and process change control and validation,
4) data trending on product performance characteristics for evaluation process control and to aid in solving product and process problems,
5)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:
Candidate must have a BS in Chemical/Mechanical/Industrial Engineering with 5-7 years of experience in a cGMP environment. In addition, at least 2 years of experience with isolator/barrier technology is highly preferred. Well developed abilities with personal computers, process automation, and project management are required. Good communication, planning, cost control, scheduling, computer, and problem solving skills are required.