Boehringer Ingelheim GmbH

We are looking for a CAPEX Manager to lead and coordinate capital investment projects at our UK site. This role is responsible for managing the full CAPEX portfolio while delivering individual engineering projects in a highly regulated pharmaceutical/bioprocessing environment. The CAPEX Manager ensures that all projects are effectively governed, fully compliant with GMP, HSE, GxP and other statutory requirements, and delivered on time and within budget. The role acts as a key interface between Engineering, Production, Quality, Procurement, Finance and external partners, ensuring investment activities support the site's long term strategy. This is a fixed-term contract until 31st December 2027. TASKS & RESPONSIBILITIES Lead the management of the full CAPEX portfolio, ensuring the master plan is always up to date (costs, schedules, priorities). Maintain full oversight of all CAPEX projects and small works, ensuring alignment with Procurement, Finance, Legal and other enabling functions. Ensure strict adherence to corporate standards, governance models and CAPEX project guidance. Establish and maintain robust controls, best practice tools, templates and methods for project delivery and portfolio governance. Communicate portfolio changes and updates to Senior Leadership Team and key stakeholders to support investment decisions. Project Execution & Delivery Act as Project Manager for assigned projects from inception through completion. Coordinate the activities of project team members, consultants, contractors and vendors. Ensure strong financial control of all capital projects, including accurate forecasting, reporting and budget adherence. Maintain compliant technical records, including qualification, validation and engineering documentation. Ensure site engineering systems and technical administrative files remain accurate and up to date. Cross Functional Collaboration Serve as the main link between Engineering, Production, Quality, Procurement, Finance, Legal and contractors. Ensure excellent communication and alignment across all project interfaces. Build strong working relationships with internal and external stakeholders. Compliance, Regulatory & EHS Ensure that all project activities fully comply with GMP, GxP, HSE, SAPO and UK statutory regulations. Conduct risk assessments and support safe execution of engineering works. Implement best practices to ensure projects enhance long term compliance and site performance. Technical Problem Solving Address engineering challenges using sound technical judgement. Support resolution of complex issues linked to utilities, cleanroom environments, biological containment and process systems. REQUIREMENTS Education Degree in an engineering discipline (Electrical, Mechanical, Civil, Chemical or Process Engineering). IOSH or NEBOSH certification. Skills & Experience Proven experience delivering CAPEX projects in highly regulated environments (ideally pharma/bioprocessing). Solid technical understanding of utilities, cleanroom/containment systems and key engineering infrastructures (e.g. HVAC, steam/clean steam, water systems, drainage). Strong financial and cost control skills, including forecasting and budget management. Ability to manage complex engineering documentation and ensure regulatory compliance. Experience with vendor management and corporate contract frameworks. Excellent communication skills and ability to work with diverse stakeholders. Strong leadership and team coordination abilities. Effective planner able to deliver projects on time and within budget. Highly autonomous, proactive and results driven. Flexible, adaptable and eager to learn. Strong problem solving and collaboration skills. Confident communicator across all organizational levels. WHY THIS IS A GREAT PLACE TO WORK Boehringer Ingelheim has been recognised as a Top Employer in the UK, demonstrating our commitment to building an exceptional workplace through strong people practices and supportive HR policies. To learn more about why BI is a great place to work, visit: A Disclosure and Barring Service (DBS) check will be required for the successful candidate. Any offer of employment will be subject to a satisfactory DBS certificate.

The MSAT Principal Expert is a senior technical role within Manufacturing Science & Technology, acting as the technical authority for bioprocessing at site level. The position supports robust, compliant, and efficient manufacturing in a highly regulated, high containment environment, directly influencing process performance, quality, and operational sustainability. The role bridges science, engineering, quality, and operations, ensuring strong process control, continuous improvement, and alignment with global MSAT standards while supporting both current manufacturing and future site development. This is a fixed-term contract till December 2027. TASKS & RESPONSIBILITIES Provide technical leadership for upstream and downstream bioprocessing operations Define, implement, and maintain best practice manufacturing standards to ensure Right First Time delivery Oversee process robustness, performance monitoring, and continuous improvement using CPV, SPC, and data trending Act as a key technical escalation point for complex deviations, investigations, and process troubleshooting Partner closely with Operations, Quality, Engineering, and Validation to embed technical and GMP standards Support CAPEX projects, technology transfers, and implementation of new processes or equipment Ensure full compliance with GMP, biosafety, EHS, and regulatory requirements Coach and mentor cross functional teams, building site technical capability Actively participate in global MSAT and SME networks, sharing best practices and leveraging global expertise Collaborate with external technology providers to introduce innovative and advanced manufacturing solutions REQUIREMENTS Education Bachelor's degree in Biotechnology, Biochemical Engineering, Biology, or a related Life Sciences discipline Advanced degree (MSc or PhD) considered an advantage Fluency in English Skills & Experience Extensive experience in biopharmaceutical or vaccine manufacturing environments Proven background in MSAT, Technical Operations, or Process Development roles Strong knowledge of GMP, biosafety, process validation, CPV, and statistical process control Knowledge of Lean / Six Sigma and continuous improvement methodologies is an advantage Ability to operate effectively in highly regulated, complex, and high containment settings Strong analytical, problem solving, and decision making capabilities Experience working across cross functional and matrix organizations with diverse stakeholders Effective communication and influencing skills at site and global level WHY THIS IS A GREAT PLACE TO WORK Boehringer Ingelheim is recognised as a Top Employer in the UK, reflecting our commitment to exceptional workplace standards, career development and a purpose-driven culture. Our employees contribute to meaningful work, creating long-term value for people, animals and the environment. A Disclosure and Barring Service (DBS) check may be required for the successful candidate. Any offer of employment will be subject to satisfactory DBS certificate.

Boehringer Ingelheim GmbH is hiring an MSAT Principal Expert for a fixed-term contract until December 2027. This senior technical role involves providing leadership in upstream and downstream bioprocessing, ensuring compliance with GMP, and driving continuous improvement in a regulated environment. The ideal candidate has a Bachelor's degree in Biotechnology or a related field, extensive experience in biopharmaceutical manufacturing, and strong problem-solving abilities. Join a company recognized as a Top Employer in the UK, committed to workplace excellence.

Boehringer Ingelheim GmbH is seeking a Senior AI Solutions Developer to design, build, and deploy AI solutions across the CRM Franchise. This role involves working with business stakeholders to translate complex problems into scalable solutions using the Microsoft stack. Candidates should have proven experience in AI solutions, particularly with Microsoft Power Platform and Azure AI. The job is based in Bracknell, UK, offering a hybrid working model of 2 days office and 3 days home.

The Senior AI Solutions Developer is a hands on technical specialist responsible for designing, building and deploying enterprise AI solutions across the CRM (Cardio Renal Metabolic) Franchise, with successful solutions designed for potential use and scaling across the wider business where appropriate. You will act as a subject matter expert in AI solution architecture on the Microsoft stack (including Power Platform, Copilot Studio and Azure AI), working with business stakeholders to diagnose complex, often ambiguous problems and translate them into scalable, high impact technical solutions. This role spans the full solution lifecycle - from discovery and design through to development, deployment and optimization - while ensuring solutions are robust, reusable and compliant with regulatory and governance standards. You will also contribute to setting technical standards, reusable patterns and best practices across the franchise. Location: Bracknell, UK (hybrid working - 2 days office / 3 days home). TASKS AND RESPONSIBILITIES Design and develop AI driven solutions (agents, automations, analytics) using Microsoft technologies. Openness to learning and adopting emerging AI tools and platforms beyond the Microsoft ecosystem. Lead discovery and solution shaping for complex, cross functional business challenges. Define end to end solution architecture, including integrations, data flows and orchestration logic. Build and deploy scalable, production ready AI solutions, ensuring technical quality and maintainability. Develop reusable technical patterns, standards and contribute to governance frameworks for AI solutions. Integrate AI solutions with enterprise systems and data sources, ensuring security and reliability. Provide technical and expert guidance to stakeholders and act as a design authority for complex use cases. Ensure all solutions meet data privacy, security and regulatory requirements within a pharma environment. REQUIREMENTS Experience & Skills Proven experience developing AI, automation or analytics solutions (typically 3+ years). Strong expertise in Microsoft Power Platform (Power Apps, Power Automate, Power BI), Copilot Studio and Azure AI. Experience designing solutions for complex or ambiguous cross functional operational challenges where requirements are not fully formed. Understanding of AI concepts (e.g. prompt engineering, retrieval augmented generation). Experience with system integration, APIs and data connectivity.Strong stakeholder engagement skills, with the ability to translate technical solutions into business value. Education Degree in Computer Science, Data Science, Engineering or a related technical field (or equivalent experience). Microsoft certifications (e.g. Power Platform) are an advantage.

Boehringer Ingelheim GmbH is seeking a CAPEX Manager to lead capital investment projects at our UK site. This role involves managing the CAPEX portfolio while ensuring compliance with all regulatory standards. The ideal candidate will have a degree in engineering and proven experience in delivering CAPEX projects within heavily regulated environments. This is a fixed-term contract until 31st December 2027, offering the opportunity to work in a highly reputable organization. Boehringer Ingelheim is noted as a Top Employer in the UK, providing a supportive workplace environment.