MES (PAS-X) Lead Engineer

MES (PAS-X) Lead Engineer at Trinity Consultants - Aztec Technologies, Inc. MES (PAS-X) Lead Engineer at Trinity Consultants - Aztec Technologies, Inc. in Black Creek, North Carolina Posted in 3 days ago.

Type:

full-time

Job Description:

MES (PAS-X) Lead Engineer (Biotech/Pharmaceutical) Location - Wilson, NC Aztec Technologies is an engineering and consulting firm providing expertise in the pharmaceutical and biotechnology industries. Aztec Technologies and Aztec Process Automation are part of Trinity Consultants Company. Trinity Consultants, Inc., a leading international EHS, life sciences and environment consulting services with 1500+ engineers worldwide. Aztec Technologies provides solutions for

Manufacturing Applications:

• Process and Facility Automation
• Project Management
• MES
• Data Analytics With offices across 3 continents, consulting firm with over 20 years of experience within the biopharmaceutical and pharmaceuticals industries.

The successful candidate will work with a group of engineers involved in the design, automation, commissioning and start-up of various processes, systems, and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill set. This is an outstanding opportunity to join our growing team and to work in the Life Sciences space that will enhance professional opportunities! Candidates need to be local or willing to relocate to the areas of operation where we have open opportunities for immediate hire in the Wilson, NC area:

Key Responsibilities:

Own MES configuration management for PAS-X, including: Manufacturing Batch Records (MBRs) Material management Equipment and timer management Label management Lead MES design, configuration, testing, and troubleshooting Act as technical interface between

MES, DCS

(DeltaV), ERP, LIMS, and other shop-floor systems Support MBR migration from a legacy site Ensure alignment with site and global MES standards Support risk assessments and GMP compliance activities Provide hands-on troubleshooting and technical support during execution Develop and maintain MES technical documentation Collaborate closely with IT, Manufacturing, Quality, and Engineering teams Required Qualifications 8+ years experience in pharmaceutical or biopharmaceutical manufacturing environments Strong hands-on experience with MES platforms, preferably Werum PAS-X Proven experience with MBR design and execution Solid understanding of GMP manufacturing processes Experience integrating MES with DCS (DeltaV) and enterprise systems Strong analytical, troubleshooting, and problem-solving skills Bachelor's degree in Engineering, IT, Science, or related discipline Preferred / Nice-to-Have Skills Programming experience: .

NET, SQL

/ PL-SQL, Java Experience with OPC servers/clients Knowledge of 21 CFR Part 11 and EU GMP Annex 11 Process knowledge across: Upstream Downstream Bioprocess support functions Ability to communicate effectively with both technical and non-technical stakeholders

Ideal Candidate Profile:

Senior-level

PAS-X MES SME

Strong on-site presence and ownership mindset Comfortable operating as Owner's Rep, not a junior configurator Deep pharma/biotech automation background Able to bridge Manufacturing, IT, Automation, and Quality