I'm currently hiring for a Mechanical Design Engineer to join a leading engineering solutions provider in thepharmaceutical and life sciences sector.This is an excellent opportunity to work oninnovative, high-spec pharmaceutical equipmentprojects from design through to completion. You'll join a collaborative engineering team where your technical expertise will have a direct impact on project success and client satisfaction.The successful candidate will be responsible for transforming client requirements into production-ready mechanical designs, leading the design process from concept through to fabrication, and supporting technical delivery throughout the full project lifecycle.Key Responsibilities:Translate client specifications and user requirements into detailed mechanical designs ready for fabrication.Produce both 3D and 2D designs using Solid Edge CAD (experience with SolidWorks or Autodesk Inventor is also advantageous).Support the sales team by creating accurate and timely sales and proposal drawings.Act as the mechanical design subject matter expert (SME) throughout all project phases.Lead stage-gate design reviews and manage the GA and P&ID approval processes with clients.Develop Bills of Materials (BoMs), source suitable components and suppliers, and collaborate with procurement and planning teams.Support the Project Manager in project scheduling and manage design variations and Change Requests (VCRs) .Provide technical support to fabrication and assembly teams, ensuring manufacturability and compliance.Assist with the creation and execution of Factory and Site Acceptance Tests (FAT/SAT) in line with GMP and GDP standards.Required Experience:Bachelor's degree (or higher) in Mechanical Engineering or related discipline.Minimum 5 years' experience in mechanical design, ideally within machine or process equipment manufacturing.Strong proficiency in Solid Edge CAD (experience with SolidWorks or Autodesk Inventor an advantage).Experience in sheet metal design, flat pattern generation, and design for manufacture .Proven ability to deliver detailed manufacturing documentation to GMP standards.Ability to manage multiple design projects simultaneously.Familiarity with ATEX, CE, UL, and machine safety standards .Knowledge of Good Documentation Practices (GDP) as applied within the life sciences sector.Demonstrated experience in both concept and detailed design of machines or automated systems.If you are looking for a new and refreshing role or have any questions about the position, then give me a call, drop me a message, or apply directly below and get ahead of the crowd I look forward to hearing from you.For a confidential discussion about this role, or to apply, send your CV to or call me, Corey Buckley, Recruitment Consultant – Head of Life Sciences – US/Europe, at Please feel free to visit my LinkedIn profile to see my references/recommendations