Key Responsibilities:
1、Design, develop, and implement MES solutions using Rockwell Pharma Suite, tailored to pharmaceutical manufacturing processes.
2、Analyze business requirements from a pharmaceutical manufacturing perspective to create detailed system specifications.
3、Provide subject matter expertise in MES systems, with a focus on Rockwell PharmaSuite, to ensure high system performance and user satisfaction.
4、Support the MES project delivery lifecycle, including planning, execution, and delivery, while ensuring compliance with pharmaceutical industry regulations.
5、Conduct system configurations, upgrades, and continuous improvements, adhering to GMP (Good Manufacturing Practice) standards.
6、 Develop comprehensive documentation for MES processes, system configurations, and SOPs (Standard Operating Procedures) specific to pharmaceutical manufacturing.
7、Deliver training programs to end-users, emphasizing best practices for utilizing Rockwell PharmaSuite in a regulated environment.
8、Manage relationships with external vendors and partners to ensure seamless system integration and data integrity.

Qualifications:
1、Bachelor’s or Master’s degree in Computer Science, Engineering, or related technical field.
2、Minimum of 5 years of experience with MES systems, specifically Rockwell PharmaSuite, in a pharmaceutical manufacturing setting.
3、Solid understanding of pharmaceutical manufacturing processes, GMP, and regulatory compliance.
4、Demonstrated project management skills with a track record of successful MES project delivery.
5、Proficiency in SQL and knowledge of programming languages commonly used in MES environments.
6、Experience with data integration and system integration in a pharmaceutical context.
7、Exceptional analytical, problem-solving, and decision-making skills.
8、Strong communication abilities and a collaborative approach to working with cross-functional teams.
9、Proficient both in spoken and written English