About Us
We unite caring with discovery to make life better for people around the world. As a global healthcare leader, our employees work together to discover and bring life-changing medicines to those who need them.
Our Mission
We put people first and give our best effort to our work. We're looking for people who are determined to make life better for people around the world.
Job Title: Senior MES Engineer - IT Manufacturing
Reports To:
Associate Director - IT Manufacturing
Job Type:
Full-time
Location:
Limerick, Ireland
About the Role
We are currently constructing a Next Generation Biotech Drug Substance Manufacturing Facility in Limerick, Ireland. This facility will be our most technically advanced manufacturing site and will include next generation manufacturing technologies and advanced data collection and analysis platforms.
Main Purpose and Objectives of Position:
The role will support and develop Manufacturing Execution System (MES) electronic batch records and logbook, associated tools, and system interfaces to fulfill business needs.
Key Responsibilities:
1. Analyze business processes and needs to recommend or implement changes to systems and/or procedures.
2. Work with local and global IT groups, automation and operations teams to support delivery of manufacturing solutions.
3. Implement solutions to meet business needs, working with site business areas and IT architects.
4. Understand how manufacturing execution systems and processes integrate with other critical systems like EWM (Extended Warehouse Management) and Delta V.
5. Provide training, documentation, and post-implementation support to users of new applications and/or systems.
6. Coordinate technical testing and installation with appropriate users and systems personnel.
7. Ensure compliance with Computer Systems Validation policies, standards, procedures, and/or practices.
8. Create and/or follow applicable procedures and standards.
Requirements:
* Bachelor's Degree in Information Technology, Computer Science, Engineering, or related field.
* 5+ years' experience in manufacturing, preferably in pharmaceutical or other regulated industries.
* Experience with Manufacturing Execution System platforms and Computer Systems Validation in cGMP regulated operations.
* Knowledge of System Development Life Cycle.
* Understanding of cGMP regulations.
* Proficiency in Microsoft Office tools.
* Project Management and leadership skills.
EEO Statement
We are dedicated to helping individuals with disabilities actively engage in the workforce, ensuring equal opportunities. If you require accommodation to submit a resume, please complete the accommodation request form. We do not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity, or any other protected status.