Join a dynamic team in one of the largest biopharmaceutical projects in the country and contribute to developing life-changing medicines.
Responsibilities and Requirements
* Proficient with Siemens PCS-7 automation software.
* Ability to program PLC systems.
* Experience with GEP and GMP automation protocols, including system upgrade requirements.
* Review and approval of FATs, SATs, DQ, IQ, and OQ protocols for GMP and critical GEP systems.
* Participation in pre-FATs, FATs, mechanical completion inspections, and SATs to ensure equipment packages are complete and correct.