At E Tech Group, joining our team means joining a group of passionate and forward-thinking experts. We’re one of the largest engineering and system integration firms in the United States providing value for our clients through IT automation and control solutions for more than 30 years to the Life Sciences, Mission Critical, Metals & Mining, Warehousing & Distribution, and CPG/Food & Beverage industries. Our national and global scale allows us to help our clients develop and implement standardized solutions at any of their facilities regardless of physical location or the local resources available at that site.
We are seeking an experienced MES Engineer – Recipe Authoring (Syncade) to design, configure, and support electronic batch records and workflows in regulated manufacturing environments. The role involves close collaboration with Manufacturing, Quality, and Engineering teams to ensure compliant and efficient MES execution.
You will:
- Develop and maintain Electronic Master Batch Records (eMBR), recipes, and workflows using MES platforms such as Emerson Syncade
- Translate process specifications and SOPs into compliant digital workflows
- Prepare and execute validation documentation and testing (IQ/OQ/PQ)
- Ensure compliance with GxP, FDA 21 CFR Part 11, and EU Annex 11
- Troubleshoot MES and recipe execution issues on the shop floor
- Manage recipe lifecycle including version control, change management, and archival
- Support integration of MES with ERP (SAP), LIMS, PLC, and SCADA systems
- Be an ambassador who embodies our Core Values, prioritizing the success of E Tech Group, our clients, and the professional development of our associates.
You have:
- Bachelor’s degree in Engineering / Computer Science or related field
- 3–7 years of experience in MES or IT application support within regulated industries
- Hands-on experience with Syncade
- Strong knowledge of ISA S88 / S95 models
- Working knowledge of SQL Server
- Good understanding of GMP and API / Biotech manufacturing
- Strong communication, analytical, and troubleshooting skills
- A DNA comprised of collaboration and teamwork.
You may have:
- Experience in pharmaceutical or biotech manufacturing environments
- Prior involvement in MES validation and regulatory audits
