Automation Engineer (MES)
PharmEng TechnologyNorth Carolina, United States
Posted December 12, 2025
Contract / Temporary
About the Company
PharmEng Technology, now part of the Efor Group, delivers specialized compliance engineering services—Commissioning, Qualification, and Validation (CQV)—to the pharmaceutical, biotechnology, and healthcare sectors, drawing on 25 years of industry expertise. The firm designs, constructs, and validates facilities, utilities, equipment, and computer systems in strict adherence to cGMP, GEP, and GLP, covering areas such as API production, laboratory, and medical device manufacturing. Leveraging Efor’s global network of 3,000 experts across 12 countries, PharmEng combines worldwide best practices with local proximity to offer flexible, innovative, and cost‑effective solutions that meet regulatory and business demands. Its culture prioritizes quality, safety, and client partnership, ensuring customized, measurable outcomes for leading industry players.
Job Description
We are seeking an experienced Automation Engineer to support the implementation and integration of DeltaV MES for drug substance manufacturing.
Requirements
- 5+ years of experience designing, configuring, and implementing Manufacturing Execution Systems
- 3+ years of experience with Emerson Syncade (DeltaV MES)
- Proficiency in debugging MES configuration
- Familiarity with cGMP standards, FDA regulations, S88 batch models, ISA 95, GAMP5, and 21 CFR Part 11