Are you ready to contribute your expertise to complex and high-impact digital transformation projects in the Pharmaceutical industry? This opportunity offers the chance to work on cutting-edge MES implementations and validation strategies within GMP-regulated environments in the UK.
Due to upcoming project needs, we are looking for a Senior Consultant – MES & Validation (Siemens Opcenter Execution Pharma PC7) to support project delivery and ensure alignment across technical, validation, and project management workstreams.
Responsibilities include, but are not limited to, the following:
- Act as a bridge between client Project Managers and delivery teams, ensuring alignment across project, technical, and validation activities
- Support coordination of MES (Manufacturing Execution Systems) activities, with a focus on Siemens Opcenter Execution Pharma
- Contribute to the definition of Validation Master Plans and overall validation strategy
- Review and assess validation documentation to ensure compliance with GMP requirements and project standards
- Evaluate the system integrator’s project methodology and assess the quality and consistency of deliverables
- Ensure alignment with project expectations, regulatory requirements, and execution standards
- Support cross-functional stakeholder management across business, IT, and quality teams
- Provide guidance on validation activities within GMP-regulated environments
- Identify project risks and propose mitigation strategies
About you:
- 7–10 years of experience in the pharmaceutical industry, with strong exposure to MES and validation activities
- Proven expertise with Siemens Opcenter Execution Pharma (PC7)
- Solid experience in project management within MES or digital manufacturing programs
- Strong knowledge of validation processes and GMP requirements
- Experience defining Validation Master Plans and validation strategies
- Ability to review and challenge system integrator methodologies and deliverables
- Strong stakeholder management and communication skills
- Experience working in cross-functional and international environments
- Knowledge of SAP and OT systems is considered a plus
- UK-based and available to work in a consulting/freelance capacity
Next Steps
Upon receiving your application, if a match is identified, you will be contacted for an initial discussion. Following a positive outcome, further discussions with the project team will be arranged. If successful, we will proceed with next steps and project onboarding. Alternatively, you will be informed if your application is not progressed.
Working with Us
By joining this project, you will be part of a dynamic and collaborative environment working on advanced MES and validation initiatives. This role offers the opportunity to engage with key stakeholders, contribute to high-value pharmaceutical projects, and play a critical role in ensuring compliant and efficient system implementation.
If you are looking for a challenging and rewarding consulting opportunity, apply now and take the next step in your career.