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Manufacturing Execution System Expert

3 weeks ago

Sligo, Sligo, Ireland beBee Careers Full time

Job Overview:

">
  • ">
  • Maintain the MES environment, author and maintain recipes and worksheets for a site.">
  • Provide technical guidance and solutioning to other MES Engineers.">
  • Act as site escalation point for complex or challenging troubleshooting or recipe design.">
  • Provide project management guidance and expertise to the MES function.">
  • Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material specifications including phase transition logic.">
  • Design, create, write and execute test and validation protocols, risk assessments, and system documentation.">
  • Ensure cleaning, equipment and product procedures are aligned to MES processes.">
  • Provide training for site personnel on their related MES roles and arrange system access.">
  • Participate in MES knowledge exchanges, MES Governance meetings, and manage issues, work-arounds and fixes identified.">
  • Liaise with Abbvie Global MES on Westport required system improvements.">
  • Support other MES system users as required to ensure business continuity.">
  • Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.">
  • Keep other recipe authors up to date on MES changes.">
  • Document all activities in line with cGMP requirements.">
  • Cross train within the team and train new team members.">
  • Participate in continuous improvement programs to implement improvements in quality, safety, environmental and production systems.">
  • Adhere to and support all EHS standards, procedures and policies.">
">

Responsibilities:

">
  • ">
  • Maintain the MES environment, author and maintain recipes and worksheets for a site.">
  • Provide technical guidance and solutioning to other MES Engineers.">
  • Act as site escalation point for complex or challenging troubleshooting or recipe design.">
  • Provide project management guidance and expertise to the MES function.">
  • Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material specifications including phase transition logic.">
  • Design, create, write and execute test and validation protocols, risk assessments, and system documentation.">
  • Ensure cleaning, equipment and product procedures are aligned to MES processes.">
  • Provide training for site personnel on their related MES roles and arrange system access.">
  • Participate in MES knowledge exchanges, MES Governance meetings, and manage issues, work-arounds and fixes identified.">
  • Liaise with Abbvie Global MES on Westport required system improvements.">
  • Support other MES system users as required to ensure business continuity.">
  • Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.">
  • Keep other recipe authors up to date on MES changes.">
  • Document all activities in line with cGMP requirements.">
  • Cross train within the team and train new team members.">
  • Participate in continuous improvement programs to implement improvements in quality, safety, environmental and production systems.">
  • Adhere to and support all EHS standards, procedures and policies.">
">

About Us:

">

We are a leading manufacturer of high-quality products, and we are committed to delivering exceptional results and exceeding customer expectations.

">

We are seeking a highly skilled MES System Administrator to join our team and contribute to our ongoing success.

">

The successful candidate will be responsible for maintaining the MES environment, authoring and maintaining recipes and worksheets, providing technical guidance and solutioning to other MES Engineers, and acting as site escalation point for complex or challenging troubleshooting or recipe design.

">

The MES System Administrator will also provide project management guidance and expertise to the MES function, design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material specifications including phase transition logic, and design, create, write and execute test and validation protocols, risk assessments, and system documentation.

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In addition, the successful candidate will ensure cleaning, equipment and product procedures are aligned to MES processes, provide training for site personnel on their related MES roles and arrange system access, participate in MES knowledge exchanges, MES Governance meetings, and manage issues, work-arounds and fixes identified, liaise with Abbvie Global MES on Westport required system improvements, and support other MES system users as required to ensure business continuity.

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This is a unique opportunity to work in a dynamic and fast-paced environment where you will have the chance to contribute your skills and experience to drive business growth and improve operational efficiency.

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If you are a motivated and experienced MES System Administrator looking for a new challenge, please submit your application.

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Requirements:

">
  • ">
  • Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.">
  • A minimum of 7 years authoring experience and has led or was technical lead on multiple implementation projects.">
  • Proficient with MES application and configuration rules and requirements including interfacing (preferably POMSnet).">
  • Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.">
  • A good knowledge of IT systems is required for this role.">
  • SAP knowledge/experience in MM, PP and IM modules.">
  • Proven attention to detail and mental concentration, ensuring total compliance with procedures.">
">

What We Offer:

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We offer a competitive salary and benefits package, opportunities for professional development and growth, and a collaborative and supportive work environment.

">

As a MES System Administrator, you will have the opportunity to work on a wide range of projects and initiatives, develop your skills and expertise, and contribute to the success of our organization.

">

We are an equal opportunities employer and welcome applications from diverse candidates.

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Please note that we do not discriminate on the basis of race, color, national origin, sex, age, disability, or any other protected status.

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We look forward to receiving your application.