Job Description

Job Scope * Execution of testing protocols (IQ, OQ) * Co-Execution vendor testing protocols (SAT) with vendor representative * Prompt highlighting of testing exceptions and issues to manageme Job Scope Execution of testing protocols (IQ, OQ) Co-Execution vendor testing protocols (SAT) with vendor representative Prompt highlighting of testing exceptions and issues to management team Prompt and concise communication of issues with project management team, as well as clear progress reporting during shift handover No management responsibilities required Primarily responsible for the maintenance and administration of GMP automation systems for the company's technical operations. This includes DCS and vendor packaged PLCs Maintenance and operation of GMP automated systems such as bioreactors, centrifuges, purification skids, and utilities Be capable of troubleshooting issues related to equipment and automation systems independently Supporting evaluation of process discrepancies, developing corrective actions, and implementing corrective actions Perform commissioning and qualification activities for automation systems Strong knowledge of Control Systems and Instrumentation and shall serve as a Subject Matter Expert for process Risk Assessments and Hazards Analyses Collaborate with other functional teams such as Manufacturing, Quality, Engineering and other functions of MSAT on cross-functional projects and responsibility e.g. Capable of leading continuous improvement projects and initiatives with involvement of other functional teams directing the activities of contract engineering personnel Requirements A degree preferable in pharmaceutical, biotechnologies or computer engineering with minimum 2 years of experience in relevant hands-on experience and industry Excellent communication and interpersonal skill Independent individual with an eye for detail EA Reg. No: R2094147 | EA License No: 19C9587