Overview:
When you join the team at Cordis, you become part of an inspiring mission to save lives, impacting millions of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart of innovation to transform cardiovascular care.
At Cordis, we’re teammates, not just employees. We embrace an empowered and one-team culture where teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients.
If you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions, then Cordis is just the place for you.
We are the people behind the people who keep saving lives.
Responsibilities:

JOB SUMMARY:

We are seeking an experienced Critical Manufacturing MES Functional Analyst, you will be responsible for the design, implementation, and support of Manufacturing Execution Systems (MES) at our company. You will work closely with both IT and manufacturing teams to ensure that MES solutions meet business requirements and are aligned with company standards and IT strategies.

PREFERRED QUALIFICATIONS:

• Experience in regulated industries such as medical devices or pharmaceuticals.
• Fluent in English and Spanish.
• Experience in deploying software projects to manufacturing.
• Project Management experience.
  

  LI-JB1

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people’s lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All our teammate’s points of view are key to our success, and we believe inclusion is everyone’s responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming

Qualifications:

• Bachelor’s degree in Engineering, Information Systems, or a related field. Equivalent experience may be considered.
• 6+ years of experience in MES implementation and support within the Manufacturing and Medical Device industry

Preferred Qualifications:

• Strong knowledge of Critical Manufacturing MES with experience in implementations, rollouts, and master data modeling/enrichment.
• Prior experience with MES implementation on multiple platforms.
• Solid understanding of Pharmaceutical/Medical Device compliance standards (21 CFR Part 11, GxP, FDA, GMP, ISO). Certification in Critical Manufacturing MES software.
• Proven experience with MES systems, preferably in a manufacturing environment.
• Strong understanding of manufacturing processes and information technology.
• Excellent problem-solving and analytical skills.
• Strong communication and interpersonal skills, capable of working collaboratively in a team environment.
• Experience with databases, SQL, and data integration techniques.
• Knowledge of programming languages such as Java, Python, or C# is a plus.
• Must be able to travel up to 25

• Act as the functional expert for Critical Manufacturing MES, bridging business requirements with technical implementation.
• Collaborate with business stakeholders, process owners, and technical teams to gather, document, and analyze requirements.
• Design, configure, and implement MES functionalities, workflows, and integrations with ERP, PLM, and other enterprise systems.
• Conduct workshops, demonstrations, and training sessions, providing knowledge transfer to end-users and internal teams.
• Support system testing (UAT, SIT), troubleshoot issues, and deliver post-go-live support.
• Document system configurations, functional specifications, and process flows for long-term maintainability.
• Analyze manufacturing requirements and translate them into functional and technical MES solutions.
• Provide ongoing support and enhancements to MES systems, improving functionality and user experience.
• Perform business process analysis and develop strategies for MES implementation.
• Customize and configure MES to meet specific stakeholder and industry requirements.
• Coordinate with development teams for any required customizations to support unique manufacturing environments.
• Facilitate review and sign-off of key deliverables with stakeholders and project teams.
• Ensure compliance with quality, safety, and regulatory standards across all MES projects.
• Work with project managers to ensure on-time delivery of solutions and implementations.
• Monitor MES system performance and address issues proactively.

Qualifications:

• Bachelor’s degree in Engineering, Information Systems, or a related field. Equivalent experience may be considered.
• 6+ years of experience in MES implementation and support within the Manufacturing and Medical Device industry.

Preferred Qualifications:

• Strong knowledge of Critical Manufacturing MES with experience in implementations, rollouts, and master data modeling/enrichment.
• Prior experience with MES implementation on multiple platforms.
• Solid understanding of Pharmaceutical/Medical Device compliance standards (21 CFR Part 11, GxP, FDA, GMP, ISO). Certification in Critical Manufacturing MES software.
• Proven experience with MES systems, preferably in a manufacturing environment.
• Strong understanding of manufacturing processes and information technology.
• Excellent problem-solving and analytical skills.
• Strong communication and interpersonal skills, capable of working collaboratively in a team environment.
• Experience with databases, SQL, and data integration techniques.
• Knowledge of programming languages such as Java, Python, or C# is a plus.
• Must be able to travel up to 25%