Job Description
An opportunity has arisen for a MES Senior Specialist to join our MES (Manufacturing Execution System) team at our state-of-the-art Dublin Biotech site within our Digital Records Design Hub. This is more than just a job. It's an exciting opportunity to be part of a team that values leadership, and an invitation to contribute to our purpose of delivering innovative health solutions worldwide.
Bring energy, knowledge, innovation to carry out the following: As a key player, you'll actively participate in the Tier process, untangling technical issues and supporting MES-related components of our manufacturing process.You'll take charge of managing MES Systems Version 3.1.8 HF5, ensuring compliance with our company policies, quality regulations, and industry standards.Overseeing vendor performance and contracts will fall under your purview, as well as supporting investigations by troubleshooting MES problems.You'll get to develop and maintain MES recipes and capabilities, collaborating with other technical functions to ensure reliable performance.You'll ensure the timely completion of the Update/Change Process, keeping aligned with quality standards.Your role will also involve MES administration and maintenance. You'll keep our automation systems in a validated state and identify opportunities for improvement.You will be responsible for developing and updating SOPs, conducting MES training, and ensuring document compliance with SDLC requirements.As part of our global team, you'll represent our company's MES team at the corporate level, contributing to our overall mission and vision.What skills you will need: In order to excel in this role, you will more than likely have:
Level 8 degree in a technical field (engineering or science) or equivalentWe need someone who can manage multiple priorities and escalate issues when necessary.A proven ability to work cross-functionally, delivering technical solutions to MES issues, is key.Strong problem-solving and troubleshooting skills will be critical to your success in this role.Knowledge of Irish, European, and International regulatory/code requirements is a must-have.Proficiency in Microsoft Office and job-related computer applications in particular SAP, along with skills in report and policy writing, will be essential.Experience in the application of Lean Six Sigma Methodology would be a distinct advantage.As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.
As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.
We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.
So, if you are ready to: Invent solutions to meet unmet healthcare needs, please apply today. Current Employees apply HERE Current Contingent Workers apply HERE Employee Status: Regular
Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements:Hybrid
Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date:11/9/2024
*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R318030
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