MES Project Manager

Cognizant Life Sciences Manufacturing

Cork

On-site

EUR 90,000 - 120,000

Full time

13 hours ago
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Job summary

Cognizant Life Sciences Manufacturing is seeking an MES Project Manager to drive delivery of Manufacturing Execution System projects across our client’s API manufacturing operations—from initial implementation through ongoing enhancement and support.

You will own end-to-end project plans, governance, and stakeholder engagement, ensuring GMP/GxP compliance and alignment with 21 CFR Part 11 while coordinating across IT, operations, and vendors to deliver robust MES solutions.

Qualifications

  • Degree in Computer Science, Engineering, Life Sciences, or a related discipline.
  • 5+ years leading project delivery, ideally in life sciences.
  • Experience delivering MES projects and knowledge of GMP/GxP.
  • Experience with Agile, Waterfall, or hybrid delivery methods.

Responsibilities

  • Own end-to-end delivery of SynCade (DeltaV MES) projects — scope, schedule, and budget — building and maintaining project plans, risk registers, and resourcing strategies as the program evolves.
  • Bring project governance into line with GxP, FDA 21 CFR Part 11, and other applicable regulatory frameworks from the outset, not as a later compliance check.
  • Coordinate delivery across business stakeholders, internal IT, vendors, and system integrators, keeping dependencies visible and on track.
  • Serve as the primary bridge between IT, operations, and regulatory/quality functions throughout the project lifecycle.
  • Run workshops and structured discussions to capture business requirements and shape system enhancements collaboratively.
  • Lead training and change management activity so MES adoption on the floor is smooth rather than forced.
  • Oversee the full MES lifecycle — design, configuration, testing, validation, and deployment.
  • Partner closely with automation, quality, and IT to deliver clean integration with DCS ad and adjacent systems.
  • Ensure every MES deliverable holds up against GMP, GxP, FDA 21 CFR Part 11 requirements.
  • Work hand-in-hand with Quality Assurance on system validation and audit readiness.
  • Keep project documentation current and structured to withstand regulatory scrutiny.

Skills

Project delivery leadership
GMP/GxP compliance
Agile/Waterfall/Hybrid delivery
Stakeholder engagement

Education

Degree in Computer Science, Engineering, Life Sciences, or related

Tools

Emerson Syncade
Körber PAS-X
Rockwell PharmaSuite
Siemens Opcenter

Job description

Role Summary We're looking for an MES Project Manager to drive delivery of Manufacturing Execution System projects across our client’s API manufacturing operations — from initial implementation through ongoing enhancement and support.

About the Role

We're looking for an MES Project Manager to drive delivery of Manufacturing Execution System projects across our client’s API manufacturing operations — from initial implementation through ongoing enhancement and support.

Responsibilities
  • Delivery & Planning
  • Own end-to-end delivery of SynCade (DeltaV MES) projects — scope, schedule, and budget — building and maintaining project plans, risk registers, and resourcing strategies as the program evolves.
  • Bring project governance into line with GxP, FDA 21 CFR Part 11, and other applicable regulatory frameworks from the outset, not as a later compliance check.
  • Coordinate delivery across business stakeholders, internal IT, vendors, and system integrators, keeping dependencies visible and on track.
  • Stakeholder Engagement & Change
  • Serve as the primary bridge between IT, operations, and regulatory/quality functions throughout the project lifecycle.
  • Run workshops and structured discussions to capture business requirements and shape system enhancements collaboratively.
  • Lead training and change management activity so MES adoption on the floor is smooth rather than forced.
  • MES Design, Build & Integration
  • Oversee the full MES lifecycle — design, configuration, testing, validation, and deployment.
  • Partner closely with automation, quality, and IT to deliver clean integration with DCS ad and adjacent systems.
  • Compliance & Documentation
  • Ensure every MES deliverable holds up against GMP, GxP, FDA 21 CFR Part 11 requirements.
  • Work hand-in-hand with Quality Assurance on system validation and audit readiness.
  • Keep project documentation current and structured to withstand regulatory scrutiny.
Qualifications
  • Degree in Computer Science, Engineering, Life Sciences, or a related discipline.
Required Skills
  • 5+ years proven track record leading project delivery, ideally within life sciences, with a strong record of hitting scope, schedule, and budget targets — MES delivery experience a strong plus.
  • Solid grounding in GMP, GxP, and the compliance landscape that governs regulated manufacturing IT.
  • Comfortable running delivery under Agile, Waterfall, or hybrid methodologies, depending on what the Programme demands.
Preferred Skills
  • Exposure to MES platforms such as Emerson Syncade, Körber PAS-X, Rockwell PharmaSuite, or Siemens Opcenter.
  • MES-to-DCS integration experience is a strong advantage.
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