Job Description Are you ready to bring your expertise, innovative thinking, and energy to a role that promises substantial impact? We invite you to join our team at our state-of-the-art Brinny site, as a Digital Records MES (Manufacturing Execution System) Senior Specialist 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.
Your Core Responsibilities 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.Who You Are You are ready if you have: Level 8 degree in a technical field (engineering or science) or equivalent.We 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, along with skills in report and policy writing, will be essential.Nice to have, but not essential: Experience in the application of Lean Six Sigma Methodology would be a distinct advantage.If you've worked in Pharmaceutical and Biotechnology manufacturing processes before, that's even better.Current Employees apply HERE Current Contingent Workers apply HERE Secondary Language(s) Job Description: 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.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.
So, if you are ready to: Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world's leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today. Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status: Regular
Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid
Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 09/23/2024
*A job posting is effective until 11:59:59PM on the day BEFORE the 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: R311755
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