MES Engineer

We are seeking a skilled MES Engineer to join our dynamic team within the pharmaceutical industry. The ideal candidate will have hands-on experience with Siemens Opcenter, strong coding capabilities, and a solid understanding of Good Manufacturing Practices (GMP). Experience with Computer System Validation (CSV) is highly desirable. We are committed to fostering a diverse, equitable, and inclusive workplace where all team members can thrive and contribute to advancing pharmaceutical manufacturing excellence. ResponsibilitiesDesign, develop, and maintain Manufacturing Execution Systems (MES) solutions using Siemens Opcenter.Collaborate with cross-functional teams including Quality, Manufacturing, and IT to ensure MES aligns with business and regulatory requirements.Perform coding tasks to customize and optimize MES workflows and functionality.Support and execute GMP-compliant processes, ensuring adherence to industry standards.Troubleshoot, analyze, and resolve MES-related issues promptly to minimize downtime.Provide training and technical support to end-users across departments.Continuously identify and implement MES process improvements to enhance operational efficiency. QualificationsProven experience as an MES Engineer with a focus on Siemens Opcenter.Strong programming/coding skills relevant to MES customization and development.Thorough knowledge of Good Manufacturing Practices (GMP) in the pharmaceutical industry.Experience in Computer System Validation (CSV) is preferred.

We welcome applicants from all backgrounds and are committed to providing equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.