Job Title: Senior MES PASX Technical Consultant for Pharmaceutical Manufacturing
Work Location: Raleigh NC/ Indianapolis IN (Onsite)
Qualifications and Requirements:
Bachelors or Masters Degree in Computer Science Information Technology Engineering Life Sciences or a related field.
Minimum 7 years of experience in MES (Manufacturing Execution Systems) implementation with an indepth focus on PASX or equivalent MES platforms in the pharmaceutical or life sciences sector.
Proven experience in PASX architecture configuration customisation and integration with peripheral systems (ERP SCADA LIMS).
Strong familiarity with Good Manufacturing Practices (GMP) and regulatory requirements including FDA 21 CFR Part 11 GxP and industry best practices.
Handson experience in advanced troubleshooting system deployment and postGo Live support within pharmaceutical manufacturing environments.
Technical Skills:
Expertlevel knowledge of PASX functionality including advanced configuration architecture and MBR design.
Strong understanding of integrations with PASX and other systems (ERP LIMS SCADA) to facilitate streamlined workflows.
Capability to analyse complex pharma manufacturing processes and translate them into comprehensive technical specifications.
Experience with system scalability performance tuning and process optimisation within PASX