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EN

Enabl3

Senior Consultant – MES Delivery

Homeoffice
Gleitzeit, Vollzeit
vor 1 Monat
Deutschland
Stellenbeschreibung

ENABL3 DOO\n\nENABL3 DOO is a fast-growing consultancy firm that specializes in digitizing shop-floor processes in the pharmaceutical industry. We are currently seeking ambitious individuals who possess significant senior project experience within the MES (Manufacturing Execution Systems) sector. As we expand globally, we are looking for driven candidates to help deliver strategic digital transformation initiatives worldwide.\n\nAs a Senior Consultant -- MES Delivery (EU based), you will work closely with our clients to understand their needs and guide them through their digital transformation journey. You will collaborate with cross-functional teams, lead workshops, and ensure successful project delivery aligned with client goals.\n\n### Key Responsibilities\n\nYou will report to the Senior Management.\n\nThis role blends MES expertise with project management to ensure successful delivery of global MES deployment programs. You will translate business requirements into scalable solutions, support decision-making, risk management and resource planning, and act as a trusted advisor to both clients and internal stakeholders.\n\nMore specifically, you will:\n\n* Lead and contribute to full-cycle MES projects from requirements gathering and functional design to testing, deployment, and post-go-live support.\n* Optimize MES solutions (e.g. PAS‑X, PharmaSuite) by identifying improvements, proposing innovative strategies, and aligning capabilities with business needs.\n* Engage directly with client at site, or remotely, depending on requirements.\n* Lead, facilitate or support cross‑functional workshops to capture objectives and constraints\n* Support project scheduling, sprint planning, resource allocation, and tracking progress against baselines.\n* Communicate effectively with technical and non‑technical stakeholders, ensuring clarity around solution design and decisions.\n* Maintain end-to-end traceability via structured documentation such as requirements lists, issue logs, and change requests to ensure compliance and traceability.\n* Develop and maintain project documentation (risk registers, RACIs, mitigation plans, progress reporting).\n* Support MES design, documentation and training in line with requirements\n\n### Qualification, Background, and Expertise\n\nWe are looking for candidates who bring:\n\n* Essential: Significant technical knowledge and hands‑on experience with pharmaceutical MES platforms (e.g., PAS‑X or PharmaSuite).\n* Languages: Excellent English (written and spoken). German, French, or Spanish are a strong advantage.\n* Communication: Exceptional ability to translate complex MES and technical concepts into clear, actionable insights, also for non‑technical stakeholders. Able to facilitate alignment between technical teams, business users, and leadership by ensuring clarity, structure, and shared understanding.\n* Project Delivery Skills: Proven experience driving structured project delivery: managing requirements, maintaining traceability, tracking issues and risks, and coordinating activities across cross‑functional teams. Demonstrated ability to ensure high‑quality outcomes within agreed timelines and scope.\n\n### Location\n\nEU countries\n\n### What We Offer\n\n* High-impact projects with global reach\n* A fast-growing environment with opportunities for professional growth\n* Competitive compensation\n* Relevant onboarding and training program to accelerate success, designed to ensure a smooth onboarding and help you build the expertise needed for success\n* Full-time position\n* Home Office work model\n* Paid business travel to client sites worldwide\n\nReady to shape the future of pharma manufacturing? Apply now and join a team that is driving innovation across the globe.