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- Tasks: Lead digital transformation projects in the Pharmaceutical industry, focusing on MES and validation.
- Company: Join a dynamic team driving innovation in pharmaceutical technology.
- Benefits: Competitive pay, flexible working options, and opportunities for professional growth.
- Other info: Engage with key stakeholders and contribute to advanced initiatives.
- Why this job: Make a real impact on high-value projects in a collaborative environment.
- Qualifications: 7-10 years in pharma with expertise in MES, validation, and project management.
The predicted salary is between 60000 - 80000 £ per year.
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.
Senior Consultant – MES & Validation employer: PQE Group
Contact Detail:
PQE Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Consultant – MES & Validation
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for opportunities. Attend industry events or webinars to meet potential employers and showcase your expertise in MES and validation.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Siemens Opcenter Execution Pharma and GMP requirements. Be ready to discuss how your experience aligns with the role and share specific examples of past projects where you made a significant impact.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation and reiterate your interest in the position. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website for the best chance at landing that Senior Consultant role! We’re always looking for talented individuals like you, and applying directly helps us get your application in front of the right people faster.
We think you need these skills to ace Senior Consultant – MES & Validation
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience with MES and validation activities. We want to see how your skills align with the specific requirements of the Senior Consultant role, so don’t hold back on showcasing your expertise!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this role. Share your passion for digital transformation in the pharmaceutical industry and how your background makes you an ideal candidate for our team.
Showcase Relevant Projects: When filling out your application, be sure to mention any relevant projects you've worked on, especially those involving Siemens Opcenter Execution Pharma. We love seeing real-world examples of your work that demonstrate your capabilities in MES and validation.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you get all the updates directly from us. Plus, it’s super easy to do!
How to prepare for a job interview at PQE Group
✨Know Your MES Inside Out
Make sure you brush up on your knowledge of Manufacturing Execution Systems, especially Siemens Opcenter Execution Pharma. Be ready to discuss specific projects you've worked on and how you contributed to their success.
✨Understand GMP Requirements
Familiarise yourself with Good Manufacturing Practice (GMP) regulations and how they apply to validation activities. Prepare examples of how you've ensured compliance in past roles, as this will show your expertise in the field.
✨Showcase Your Project Management Skills
Be prepared to talk about your project management experience, particularly in MES or digital manufacturing programmes. Highlight any methodologies you've used and how you've managed cross-functional teams to achieve project goals.
✨Engage with Stakeholders
Demonstrate your strong communication skills by discussing how you've effectively managed stakeholder relationships in previous roles. Share specific instances where you acted as a bridge between technical teams and project managers to ensure alignment.