MES Engineer

Overview The MES Engineer is a technical contributor responsible for the configuration, implementation, and support of Manufacturing Execution System (MES) solutions within the Devens Cell Therapy Facility. This role focuses on recipe authoring, troubleshooting, and system maintenance in Emerson Syncade MES, ensuring reliable and compliant system operation. The MES Engineer works closely with manufacturing, quality, and IT teams to support day-to-day operations, resolve issues, and contribute to the continuous improvement of digital manufacturing systems. Responsibilities MES Configuration & Recipe Authoring: Configure, modify, and maintain MES recipes to meet business requirements. Document and test changes while following governance procedures to ensure accuracy and compliance. Operational Support: Provide hands-on support for MES issues affecting manufacturing operations. Collaborate with IT and operations to troubleshoot and resolve incidents. Participate in rotational on-call support to ensure uninterrupted manufacturing activities. Business Process Understanding: Develop a working knowledge of assigned manufacturing processes. Assist in investigations and contribute to recipe improvements that enhance operational efficiency. Compliance & Documentation: Ensure MES solutions comply with cGMP, 21 CFR Part 11, Annex 11, and internal quality standards. Maintain accurate technical documentation, test records, and validation deliverables. Training & Knowledge Sharing: Support the creation of training materials for MES recipes and workflows. Provide guidance to new MES users or recipe authors as needed. Contribute to the design, testing, documentation, and deployment of MES solutions of moderate complexity, while providing operational support to end-users. Qualifications Education: Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field. Experience: 1–3 years of experience with MES systems in Biologics, Pharmaceutical, or Cell/Gene Therapy industries. Exposure to Emerson Syncade MES or a comparable MES platform preferred. Understanding of cGMP regulations and computerized system validation. Skills: Strong problem-solving ability and attention to detail. Effective communication skills and ability to collaborate with cross-functional teams. Interest in recipe authoring, troubleshooting, and continuous improvement. Other Willingness to participate in rotational on-call support for manufacturing operations. Compensation & Benefits Devens - MA - US: $89,390 - $108,315. The starting compensation range for a full-time employee (FTE) is listed above. Additional incentive cash and stock opportunities (based on eligibility) may be available. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary by job and location. For more on benefits, please visit Benefits include health coverage, wellbeing programs, retirement and disability protections, and other offers. Some benefits are subject to plan terms and enrollment. Details vary by location and role. Work Arrangements & Accessibility BMS occupancy structure defines whether work is site-essential, site-by-design, field-based, or remote-by-design. Site-essential roles require 100% onsite shifts; site-by-design roles may allow hybrid work with at least 50% onsite; field-based/remote roles require travel and are defined as essential functions. BMS is committed to equal employment opportunity and to providing accommodations in the recruitment process and in the workplace. If accommodations are needed, contact View email address on click.appcast.io. Data Protection & Candidate Rights : We do not request payments or sensitive information during recruitment. Some roles may involve background checks as permitted by law. For more information on data protection and candidate rights, visit the company sites linked in the original posting. #J-18808-Ljbffr Bristol Myers Squibb