Position Overview
In This Role, Your Responsibilities Will Be:
Recipe Authoring HRML, XML, VB Script Database : SQL GAMP, FDA validation and 21CFR part 11 compliance Pharmaceutical manufacturing process Who You Are: You promote high visibility of shared contributions to goals. You quickly and significantly take action in constantly evolving, unexpected situations. You actively seek input from pertinent sources to make timely and well-informed decisions. You handle the risk that comes with moving forward when the outcome is not certain. For This Role, You Will Need: Total experience of 4- 10 years in Automation / MES MES experience at least 2 years. Hands on experience on MES systems like Rockwell, Werum, Siemens, ABB Hands on experience on Pharmaceutical Batch automation projects. Preferred Qualifications That Set You Apart: Bachelor of Engineering Computers / Electronics/Instrumentation from reputed university ...