What are the responsibilities and job description for the Senior MES PAS-X Technical Consultant for Pharmaceutical Manufacturing position at Apptad Inc?
Job Title: Senior MES PAS-X Technical Consultant for Pharmaceutical Manufacturing
Work Location: Raleigh, NC/ Indianapolis, IN (Onsite)
Work Location: Raleigh, NC/ Indianapolis, IN (Onsite)
Qualifications and Requirements:
Bachelor's or Master's 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 in-depth focus on PAS-X or equivalent MES platforms in the pharmaceutical or life sciences sector.
Proven experience in PAS-X 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.
Hands-on experience in advanced troubleshooting, system deployment, and post-Go Live support within pharmaceutical manufacturing environments.
Bachelor's or Master's 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 in-depth focus on PAS-X or equivalent MES platforms in the pharmaceutical or life sciences sector.
Proven experience in PAS-X 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.
Hands-on experience in advanced troubleshooting, system deployment, and post-Go Live support within pharmaceutical manufacturing environments.
Technical Skills:
Expert-level knowledge of PAS-X functionality, including advanced configuration, architecture, and MBR design.
Strong understanding of integrations with PAS-X 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 PAS-X
Expert-level knowledge of PAS-X functionality, including advanced configuration, architecture, and MBR design.
Strong understanding of integrations with PAS-X 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 PAS-X
