Full job descriptionYou will be responsible for translating customer requirements into clear, accurate and manufacturable engineering drawings for bio- processing systems.
Client Details
My client is a global provider, supporting the life sciences sector with innovative single-use technologies, helping customers improve efficiency and quality in regulated environments.
Description
*Convert customer requirements, specifications and discussions into clear and manufacturable engineering drawings
*Create and maintain detailed 2D and 3D models and assemblies in SolidWorks
*Serve as the interface between customers, sales and manufacturing
*Ensure all drawings meet internal standards for quality, completeness and traceability
*Review and update drawings based on feedback
*Support Design for Manufacturing (DFM) efforts, ensuring designs are optimised for production and assembly
*Maintain accurate Bills of Materials (BOMs) and support engineering change processes through PLM/ERP system.
*Participate in design reviews and provide input to improve clarity, consistency, and usability of engineering documentation
*Identify opportunities to standardise designs and improve drawing efficiency and repeatability
* Support continuous improvement initiatives related to drawing quality, turnaround time, and cross-functional communication
Monday- Friday (Days Role)- 5 days on site
Profile
*Recognised Engineering Qualification
*Experience translating customer requirements into engineering drawings and technical documentation
*Advanced proficiency in SolidWorks, including part modelling, assemblies, and drawing creation
*Experience supporting or leading transitions to standardized CAD systems and workflows
*Strong understanding of manufacturing methods, particularly for plastic assemblies and fluid handling systems
Desired but not mandatory experience:
*Familiarity with ISO 13485, cGMP, and/or other regulated quality systems
*Knowledge of ASME, ISO, or similar drawing and design standards
*10+ years of experience in design engineering or drafting within a regulated manufacturing environment
*Minimum 5+ years of experience in medical device, bioprocessing, or similarly regulated industries (ideally with experience in single-use products)
Job Offer
*Competitive salary
*25 days holiday plus bank holidays
*Royal London pension (4% employer / 4% employee)
*Employee incentive bonus
*Employee wellbeing resources