A high-growth pharmaceutical company is seeking a full-stack developer for a new AI function. As the first hire for the Ireland AI Hub, you will design and deploy AI automations that impact various workflows. The ideal candidate has experience with Python and JavaScript, and strong knowledge of LLM integration. This role offers a flexible, remote-first environment and the opportunity to significantly accelerate drug commercialization timelines. #J-18808-Ljbffr
A high-growth pharmaceutical company is creating a new AI function to accelerate rare-disease drug commercialization. This is a greenfield role —you will design, build, and deploy AI automations from scratch, directly impacting regulatory, commercial, and operational workflows. This Role Offers You Ownership of the Ireland AI Hub as the first hire Build LLM-powered agents and production-ready automations Work with cutting-edge infrastructure including an NVIDIA DGX Spark Significantly accelerate commercialization timelines for life-saving therapies Flexible, remote-first environment in a fast-moving, small team Responsibilities Develop full-stack AI systems (Python + JavaScript/TypeScript) and APIs Integrate LLMs and design agentic workflows for regulatory, commercial, and internal operations Deploy and maintain AI sandbox, automations, and workflow pipelines Collaborate with business teams to translate complex problems into actionable AI solutions You Will Bring Proven full-stack development experience with Python (FastAPI/Flask) and JavaScript/TypeScript (React/Vue/Node.js) Strong knowledge of LLM integration, workflow automation, and database systems (PostgreSQL, vector DBs) Comfortable with Linux/Docker, system setup, and prototyping quickly Entrepreneurial mindset, solution-oriented, able to communicate technical concepts clearly to non-technical stakeholders #J-18808-Ljbffr
About the Company A fast-growing European biopharma organization at the forefront of rare disease medicine commercialization. Operating across 40+ markets, the company accelerates the path from regulatory approval to patient access—cutting timelines in half compared to traditional pharma. With a mission to make life-saving therapies available faster, they’re now investing in AI to redefine how medicines reach the market. The Opportunity Join a newly formed AI & Digitalization function and take ownership of building the company’s AI infrastructure from the ground up. As one of the first hires in this division, you’ll design, deploy, and scale MLOps pipelines that power intelligent automation, large language model integrations, and real-world healthcare applications. This is a greenfield role with full autonomy—no legacy systems, no red tape, and huge scope for impact. Key Responsibilities Architect and maintain cloud-based AI/ML infrastructure (Azure preferred, but AWS/GCP welcome). Develop ETL/ELT data pipelines and manage orchestration for large-scale AI workflows. Automate deployment, monitoring, and retraining of machine learning models. Build integrations using REST APIs, event-driven systems, and secure authentication frameworks. Collaborate cross-functionally to translate real business needs into scalable, compliant AI systems. Essential Skills 2+ years’ experience with Kubernetes (AKS, EKS, or GKE) and Infrastructure-as-Code (Terraform). Proven Python skills for orchestration, automation, and tooling. Strong background in CI/CD (GitHub Actions, GitLab, or Azure DevOps). Experience with data engineering tools (Azure Data Factory, Synapse, or similar). Solid understanding of MLOps frameworks (MLflow, model monitoring, experiment tracking). Nice-to-Haves Exposure to LLMs, RAG, and vector databases (OpenAI, Hugging Face, Langfuse). Experience in pharma or regulated industries (GxP, GDPR, 21 CFR Part 11). Familiarity with low-code automation tools (n8n, Make.com, Zapier). You’ll Thrive If You Are: A proactive builder who loves working on greenfield projects. A fast mover who prototypes and iterates quickly. A clear communicator comfortable bridging technical and non-technical teams. Entrepreneurial, curious, and motivated by meaningful impact in healthcare. #J-18808-Ljbffr
An innovative organisation within the life sciences sector is seeking a junior-to-mid-level AI Engineer to support its digital transformation strategy. This is a unique opportunity to apply your technical expertise to impactful real-world challenges - building intelligent systems that streamline operations, enhance data-driven decision-making, and drive business efficiency. This Role Will Offer You The chance to shape and implement AI solutions across a growing, forward-thinking company Exposure to end-to-end AI development , from rapid prototyping through to deployment A collaborative environment where innovation, autonomy, and problem-solving are encouraged Your Responsibilities Design, develop, and deploy AI and ML prototypes to solve operational challenges Collaborate with technical leadership on solution architecture and cloud infrastructure Leverage data platforms such as Azure, Databricks, and Snowflake to manage and optimise data flows Build and maintain scalable AI pipelines using Python , LangChain , and MLOps best practices Continuously evaluate new technologies and approaches to improve performance and efficiency You Will Bring Proven experience with Python and AI/ML frameworks Hands-on exposure to LangChain , cloud environments (Azure or similar), and MLOps tools Understanding of data architecture , virtual private clouds , and modern AI stacks A startup mindset — self-driven, adaptable, and eager to build quickly and iterate Strong problem-solving skills with the ability to work across technical and business teams #J-18808-Ljbffr
Role Overview We are seeking an experienced CQV (Commissioning, Qualification & Validation) Lead to support a GMP manufacturing facility in Cork. The successful candidate will provide technical leadership and oversight for CQV activities, ensuring all systems, utilities, and equipment are commissioned and qualified in line with project timelines, industry standards, and regulatory requirements. This is a 6-month contract role, ideally suited to a candidate with strong CQV leadership experience in GMP environments. Key Responsibilities Lead the planning, coordination, and execution of CQV activities across assigned systems and equipment. Develop and review CQV deliverables, including protocols (IQ/OQ/PQ), test scripts, and summary reports. Ensure compliance with GMP, FDA, EMA, and ICH guidelines throughout all qualification and validation phases. Oversee contractor/vendor activities related to CQV execution. Manage deviations, change controls, and CAPAs arising from CQV execution. Interface with project engineering, quality, manufacturing, and automation teams to drive project progress. Support regulatory inspections and audits, providing CQV expertise and documentation as required. Ensure project milestones are met within scope, schedule, and budget. Mentor junior CQV engineers and provide technical guidance. Qualifications & Experience Bachelor’s degree (or higher) in Engineering, Science, or related discipline. 8+ years’ experience in Commissioning, Qualification, and Validation within the pharmaceutical/biopharma industry. Proven track record in leading CQV activities for GMP facilities, including utilities, process equipment, and/or cleanrooms. Strong understanding of regulatory requirements (FDA, EMA, cGMP, ASTM E2500, ISPE guidelines). Experience managing cross-functional teams and external vendors/contractors. Excellent problem-solving, communication, and organizational skills. Ability to work independently while driving project deliverables under tight deadlines. #J-18808-Ljbffr
Job Title: Mechanical Project Engineer Location: Cork, Ireland We are seeking an experienced Mechanical Project Engineer to join a Capital Projects team in a leading pharmaceutical and medical devices environment. This role will play a key part in delivering complex engineering projects in a live operational site. Key Responsibilities Lead and manage capital projects from design through construction to handover. Coordinate with contractors, suppliers, and design consultants to ensure compliance with project scope, timelines, and regulations. Review and approve design documentation, ensuring alignment with agreed project milestones. Oversee on-site construction works, ensuring compliance with safety, quality, and environmental standards. Communicate project status and updates effectively to stakeholders. Ensure smooth transition of work packages from design to operations in a live environment. Qualifications & Experience Degree in Engineering with at least 10 years’ experience in capital projects within pharmaceutical or medical device sectors. Registered with a professional engineering body (e.g., IEI or equivalent). Strong background in project and construction management, including regulatory compliance. Skilled in Microsoft Office and project management tools. Proven ability to lead multidisciplinary teams and manage change. Solid knowledge of construction methods, safety regulations, and industry standards. Preferred Experience Knowledge of Powder Transfer Systems, HCl systems, and ATEX regulations. Familiarity with AutoCAD, Revit, and other design software. Experience with value engineering and cost-saving measures. This is a senior role suited to an experienced engineer who thrives in a dynamic, regulated, and high-performance environment. #J-18808-Ljbffr
