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| Job Location | Blackpool |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
CK Group are recruiting for a Design Quality Engineer to join a company in the Pharmaceutical industry at their site based in Blackpool on a on a contract basis for 12 months.Company:Our client has one of the worlds most comprehensive portfolios of orthopaedic and neuro products and services for joint reconstruction, trauma, spine, sports medicine, neuro, cranio-maxillofacial, power tools and biomaterials.Location: This Design Quality Engineer role will be based at our clients site in Blackpool, Lancashire. Salary: Hourly £32.20 PAYE or £42.49 LTD.Design Quality Engineer Role:- Support risk assessment activities: Develop and utilise DFMEA/PFMEA and other QA risk analysis techniques in order to minimise potential risk during development/implementation activity.- Ensure effective problem analysis/complaint investigation (CAPA) as required and define through negotiation effective corrective actions.- Produce quality process specifications as required during the development and implementation of new products. Approve design specifications (e.g. drawings, protocols) as defined for own scope of responsibility.- Work with relevant business stakeholders, support and lead in the Non-Conformance (NC),Corrective And Preventative Action (CAPA) investigations and general problem solving for both design and process.- Compile and execute validation protocols for new product/processes. Assist in resolving all quality issues, allowing transfer of manufacturing processes to Operations.Your Background:- Previous experience with reporting into business stakeholders, supporting and leading in the Non-Conformance (NC), Corrective And Preventative Action (CAPA) investigations and general problem solving for both design and process.- You will have the ability to document and maintain in good order all relevant Quality documents.- Previous experience of compiling and executing validation protocols for new product/processes.- The ability to work cross-functionally to ensure adequate design inputs are included in product development or change projects.- Previous experience of working in the medical device industry is preferred but not essential.Apply:For more information or to apply for this Design Quality Engineer position, please contact CK Group, quoting job ref 48064.It is essential that applicants hold entitlement to work in the UK.