|Looking for a candidate with a background in mechanical or automation engineering.
Self-starter and takes initiative, be assertive, and manage schedule on assigned projects from inception to completion.
Able to manage and solve complex problems with limited guidance.
A working knowledge of the Bio-Pharmaceutical industry is beneficial.
Possess experience with process development in a lean manufacturing area.
Can write and execute protocols including installation qualifications (IQ), operational qualification (OQ) and performance qualification (PQ).
In addition, they should have experience in composing work instructions and can provide guidance and training to others.
Candidate should have experience working in a ISO-13485/9000 cGMP ISO 7 clean room environment.
Candidate should have a strong work ethic that will drive results in an expeditious manner towards a positive outcome.
Can collect and interpret data to develop capable manufacturing process that will yield a consistent quality product repeatedly.
Additional skills in web converting/handling, heat sealing and system automation is a plus.
Qualifications would consist of a bachelor degree or equivalent experience