Conduct product and production failure investigations implementing corrective actions and preparing sound scientific reports. Conduct technical projects 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) the 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) must be highly motivated individual will take ownership of the process/product they support to provide guidance and upgrades to the manufacturing group.
Requirements: Must have 5-7 years of experience in a cGMP environment. At least 2 years of experience with isolator/barrier technology is highly preferred. Solid computer skills, process automation and project management are required. Good communication planning cost control scheduling computer and problem solving skills are required.
• EDUCATION: BS in Chemical/Mechanical/Industrial Engineering
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