Analyst I Information Technology (United States)

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.

Job Summary

As an Analyst I, 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.

Key Responsibilities

• Analyze manufacturing needs and convert them into functional and technical requirements for MES solutions.
• Design, configure, and implement MES applications and interfaces with other enterprise systems.
• Provide ongoing support and enhancements to existing MES systems to improve functionality and user experience.
• Support user training sessions and create user manuals and documentation for MES solutions.
• Work with project managers and other stakeholders to ensure timely delivery of projects and solutions.
• Monitor MES system performance and resolve any issues or discrepancies reported by users.
• Perform business process analysis – elaborate strategies and plans for product implementation.
• Understand the specific stakeholder requirements and map them to solutions available in the Critical Manufacturing MES.
• Create configurations and customizations specific for given stakeholders.
• Perform demonstrations of the solution tailored to the stakeholder specific requirements.
• Coordinate custom developments which might be required to fulfill specific manufacturing environments.
• Ensure the smooth communication between the stakeholders and the implementation and development teams.
• Facilitate the reviews and signoff of key deliverables and milestones between the project team and the business stakeholders.
• Oversee implementation, deployment and user training activities.
• Ensure compliance with all applicable quality, safety, and environmental regulations.

Required:

• Associate degree required; equivalent experience considered 
• 1-2 years related experience
• Working experience in managing Critical Manufacturing MES implementations and Rollouts, master data modelling and enrichment.
• Previous work experience in MES implementation using any platform.
• Must have basic knowledge or understanding of Pharmaceutical/Medical Device compliances like 21 CFR Part 11 Compliance, GxP etc.