MES Engineer (Tempo/Syncade)

MES Engineer (Tempo/Syncade)Location: Norwood, MA (Onsite)Duration: 6+ MonthsWork Authorization: H1B Accepted (Strong Candidates)Position OverviewWe are seeking an MES Engineer with hands-on experience in Tempo/Syncade MES and system integrations to support pharmaceutical manufacturing operations. The ideal candidate should have strong MES system expertise, particularly around system integration, along with experience in regulated pharmaceutical or biotechnology environments.Key ResponsibilitiesConfigure, support, and maintain MES platforms, including Tempo, Syncade, or equivalent systems.Design and support MES integrations with manufacturing and enterprise systems.Collaborate with manufacturing, automation, and IT teams to ensure seamless system functionality.Support MES implementation, troubleshooting, and continuous improvement initiatives.Assist with system validation activities in compliance with GxP, GAMP, and Computer System Validation (CSV) requirements.Develop and maintain system documentation, configuration records, and technical specifications.Participate in issue resolution, testing, and deployment of MES enhancements.Ensure system reliability and compliance within pharmaceutical manufacturing environments.Required Qualifications2–4 years of experience with MES systems, preferably within Drug Product manufacturing in pharmaceutical or biotechnology environments.Experience with MES platforms such as Tempo, Syncade, or equivalent systems.Strong understanding of MES system architecture and system integrations.Basic understanding of GxP regulations, GAMP guidelines, and Computer System Validation (CSV).General knowledge of manufacturing processes, automation systems, and systems integration principles.Familiarity with programming concepts or languages such as SQL, Python, or C#.Strong analytical, troubleshooting, and communication skills.Preferred QualificationsExperience integrating MES with enterprise and manufacturing systems.Knowledge of pharmaceutical manufacturing processes and automation technologies.Experience working in regulated life sciences environments.