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JOB TITLE: Design Engineer RESPONSIBLE TO: Engineering Manager LOCATION: Flexible (Warwick HQ, occasional national and international travel) OBJECTIVE: To execute engineering work at a high level of competence and constantly refine engineering processes and methods. Collaborating with both internal and external customers to ensure robust, efficient, and manufacturable designs that meet project and client need. NATURE OF THE WORK • Mechanical system design and development for shades, including but not limited to blinds and facades, • New Product Introduction from concept to production, • Working with the internal team, as well as clients, suppliers, manufacturers and contractors, • System Design and Development, • Design of Production Equipment, • Working with architectural and engineering drawings, • Design of experiments and modelling system behaviour, • Broad experience and understanding of an array of manufacturing techniques, particularly in relation to moving parts, • Training and developing junior engineers MAIN RESPONSIBILITIES • Maintaining consistently high-quality output from the engineering department by leading concept generation and design activities, providing engineering support to all parts of the business., • Oversight of major projects, • Leading manufacturing processes and technology improvement activities, • Defining, maintaining, and improving engineering and business processes in line with industry best practice., • Launch feasibility studies for new project requests., • Provide innovative and robust designs to new projects as well as new products to be mass-manufactured., • Apply manufacturing engineering / design for manufacture expertise to creating efficient manufacturing methods and tools for existing and new products., • Mentor, support, and train junior engineers., • Maintain and improve internal engineering processes., • Troubleshooting manufacturing, product performance, and installation issues., • Design of experiments to evaluate and characterise component and system performance and behaviour., • Ensure project documents are complete, current, and appropriately stored and shared., • Identify risks and plan for successful delivery., • Advise the Specification team on our delivery capabilities and collaborate with pitching team to win new projects. PERSON SPECIFICATION Skills & Characteristics • Extremely resourceful., • Strong interpersonal and customer-facing skills, able to build effective relationships with clients, suppliers, and contractors., • Exceptional time management and organisation skills with the ability to juggle multiple tasks at once., • A good communicator with effective stakeholder management & conflict resolution skills., • Be a good team player and an effective leader who motivates colleagues to work together to deliver results, • Meticulous record keeper who ensures everyone delivers on their commitments., • Pragmatic problem solver who always gets the job done., • Practical, hands-on problem solver with a track record of delivering mechanical solutions in construction. Knowledge & Experience • Strong background in mechanical engineering for construction products (ideally with moving parts such as doors, windows, and façades)., • CAD and CAM software, (SolidWorks preferred), • Design for Manufacture & Assembly, • Experience collaborating with construction product manufacturers., • Modern Methods of Manufacture (CNC/CAM, Additive, Laser Processing, Robotics and special purpose machines), • Experience working with architectural and engineering drawings to integrate mechanical solutions into building projects., • Leading engineering development activities – FMEA, Concept and Design Reviews, New Product Introduction, Risk Registers etc.

Senior Mechanical Engineer – Medical Devices Warwick Full-time Permanent A rare opportunity has arisen for an exceptional Senior Mechanical Engineer to join a world-leading technical design consultancy specialising in the development of advanced, safety-critical medical devices. This role offers the chance to shape next-generation healthcare technologies, taking products from first principles through to market launch and making a direct impact on patient outcomes. You will collaborate closely with highly skilled engineers, scientists, and designers, solving complex technical challenges and delivering devices that meet the highest standards of performance, safety, reliability, and regulatory compliance. Key Responsibilities: • Lead mechanical engineering work packages within the development of novel medical devices, ensuring rigorous adherence to regulatory frameworks (ISO 13485, ISO 14971, IEC 60601, etc., as relevant)., • Develop complete mechanical architectures for devices including mechanisms, enclosures, actuators, fluid systems, and precision assemblies., • Produce high-quality CAD using SolidWorks, establishing robust design intent and managing complex assemblies., • Perform simulation-driven engineering using ANSYS (FEA) and CFD to assess structural integrity, thermal behaviour, fluid dynamics, and overall system performance., • Drive iterative development using rapid prototyping tools and techniques (SLA, SLS, FDM, CNC machining, soft tooling) to accelerate verification cycles., • Engineer components and assemblies optimized for high-volume production, particularly injection moulding, automated assembly, and DFM/DFA best practice for medical devices., • Lead design reviews, mentor junior engineers, and ensure engineering excellence across all technical outputs., • Communicate clearly with clients, regulatory teams, and internal stakeholders, providing authoritative technical insight and documentation. Requirements: • Degree in Mechanical Engineering (1st or Upper 2nd class) or equivalent highly technical discipline., • Substantial and demonstrable experience in medical device design is essential. Candidates without medical-device experience will not be considered., • Strong working expertise in SolidWorks for complex 3D modelling, mechanisms, and controlled documentation., • Proven experience using ANSYS (FEA) and CFD tools for simulation-led design and verification., • Deep understanding of medical device development processes, including risk management, design controls, verification/validation, and regulatory considerations., • Hands-on experience with rapid prototyping, testing, and iteration to meet stringent performance and safety requirements., • Strong understanding of high-volume manufacturing techniques, especially injection moulding, and how they apply to regulated medical products., • Excellent problem-solving ability, attention to detail, and a proactive, ownership-driven mindset., • Ability and eligibility to work on-site in the UK as required. What You Can Expect: • Work on high-impact medical device programmes that progress to market and improve patient lives., • Direct involvement in mechanism design, prototyping, verification testing, and design-for-manufacture decision-making., • The chance to create novel IP, help shape device architecture, and influence core technical strategy., • Structured professional development, mentoring, and progression opportunities within a world-class consultancy environment., • Competitive salary with paid overtime., • 22 days holiday (increasing with service), plus additional holiday bonuses., • 37-hour working week with half-day Fridays., • Annual discretionary bonus and fixed holiday bonuses., • Pension scheme and cycle-to-work program., • Social events and sports clubs for team engagement., • Consideration for hybrid working arrangements.