ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients’ needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com. We are seeking a mid-level MES Engineer with hands-on experience in Emerson Syncade and working knowledge of DeltaV systems to support MES implementation and validation activities in a GMP-regulated pharmaceutical manufacturing environment. This role is focused on test script development and execution, EBR support, and integration testing across MES and process automation platforms. The ideal candidate is detail-oriented, familiar with pharmaceutical validation standards, and capable of working cross-functionally with QA, manufacturing, and IT/automation teams. Key Responsibilities: Develop, review, and execute IQ/OQ/PQ test scripts for MES deployments using Emerson Syncade. Support validation deliverables including traceability matrices, deviation documentation, and test summary reports in alignment with GAMP 5 and 21 CFR Part 11 requirements. Assist in the design, testing, and troubleshooting of electronic batch records (EBRs) in Syncade based on pharmaceutical manufacturing processes. Participate in MES–DeltaV integration testing, including data exchange validation and automated batch execution workflows. Work closely with QA and validation teams to ensure compliance with GMP standards and internal quality procedures. Provide support during system go-lives, ensuring smooth transition to operational use and effective issue resolution. Maintain accurate documentation for all MES-related activities in line with regulatory expectations. Requirements Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related field. 2–5 years of experience working with Emerson Syncade MES in a pharmaceutical GMP environment. Familiarity with DeltaV DCS and integration between MES and automation platforms. Strong experience authoring and executing CSV documentation and test scripts. Understanding of pharmaceutical manufacturing processes such as batch production, equipment tracking, and materials management. Excellent written and verbal communication skills, with attention to documentation and regulatory detail. Preferred Qualifications: Experience supporting MES validation in sterile, biologics, or oral solid dosage manufacturing. Hands-on involvement in greenfield or brownfield MES deployment projects. Basic understanding of SQL, XML, or data interfaces used in MES/automation integration. Knowledge of ALCOA+ principles, data integrity, and computerized system lifecycle. Benefits What We Offer: Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience. Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment. Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.

Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.