Senior Mes Project Manager

Our Client

Barcelona

On-site

EUR 90,000 - 120,000

Full time

14 days+

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Job summary

Our Client in Barcelona, Spain, seeks a Senior MES Project Manager to lead complex manufacturing execution projects in the pharma sector. You will drive MES implementations, interfaces and upgrades across production environments, coordinating IT, Operations, Quality and Regulatory teams.

You will ensure GMP, FDA and EMA compliance, manage budgets and risks, mentor junior PMs, and report to senior stakeholders. The role starts ASAP on a 12+ month contract and requires EU-based eligibility.

Qualifications

  • 5+ years' Project Management experience, including MES projects.
  • 3+ years leading MES projects in pharma/ Life Sciences.
  • Strong SAP MES experience across implementation, interfacing, configuration and optimisation.
  • Knowledge of GMP and regulatory requirements.
  • Proven ability to manage multi-site, cross-functional teams, budgets and risks.

Responsibilities

  • Lead end-to-end MES implementation and upgrade projects.
  • Manage project plans, budgets, resources, risks and dependencies.
  • Coordinate IT, Operations, Quality and Regulatory teams.
  • Analyse manufacturing processes to identify optimisation opportunities.
  • Ensure compliance with GMP, FDA and EMA requirements.
  • Mentor junior project managers and report to senior stakeholders.

Skills

SAP MES
Project Management
GMP compliance
Pharma/Life Sciences
Stakeholder management
Budget management
Multi-site projects

Education

PMP/PRINCE2 certification

Tools

SAP
SAP S/4HANA

Job description

Senior MES Project Manager - Pharma


ASAP Start | 12+ Month Contract - Must be EU based


We're supporting a leading pharmaceutical organisation looking for an experienced Senior MES Project Manager to lead complex manufacturing execution, integration and optimisation projects across its production environment.
This is an excellent opportunity for an experienced SAP MES Project Manager to work across IT, Manufacturing, Quality and Regulatory teams, delivering transformation initiatives that improve manufacturing efficiency while ensuring compliance with pharmaceutical standards.

Key Responsibilities
  • Lead end-to-end MES implementation, interface and upgrade projects.
  • Manage project planning, budgets, resources, risks and dependencies.
  • Lead cross-functional teams across IT, Operations, Quality and Regulatory.
  • Analyse manufacturing processes and system performance to identify optimisation opportunities.
  • Ensure projects comply with GMP, FDA and EMA requirements.
  • Lead risk assessment, mitigation and change management activities.
  • Manage senior stakeholder communications, reporting and project governance.
  • Support business adoption and mentor junior project managers.
Required Experience
  • 5+ years' Project Management experience, including at least 3 years managing MES projects.
  • Strong SAP MES experience across implementation, interfacing, configuration/customisation and optimisation.
  • Proven pharmaceutical or Life Sciences experience.
  • Strong understanding of pharmaceutical manufacturing processes and GMP/regulatory requirements.
  • Experience managing complex, multi-site projects and cross-functional teams.
  • Strong stakeholder management and communication skills.
  • Experience with budget management and resource planning.
  • PMP, PRINCE2 or equivalent certification is advantageous.
Desirable
  • SAP S/4HANA implementation experience
  • Lean Six Sigma or equivalent process improvement experience.
  • Change management and organisational transformation experience.
  • Experience managing multiple pharmaceutical manufacturing sites or global project portfolios.
Contract Details


Start: ASAP - within 4 weeks
Duration: 12 months minimum
Sector: Pharmaceutical / Life Sciences

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