You 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 ranging from £55,000 to £60,000 per annum
- 25 days holiday plus bank holidays
- Royal London pension (4% employer / 4% employee)
- Employee incentive bonus
- Employee wellbeing resources
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