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Job Title Location Salary  
Chemical Process Engineer Sligo Not Disclosed
Process Development Manager Dublin North €80000 - €100000
Senior Process Engineer Dublin North Not Disclosed
Snr Process Engineer Dublin North Not Disclosed
Senior Process Development Scientist Dublin North €65000 - €70000



Other Medical Device Jobs

Job Title Location Salary  
Operational Excellence & API Support Leader Sligo Not Disclosed
Tech Transfer Scientist Dublin South Not Disclosed
Quality Systems Engineer. Westmeath Not Disclosed
Operational Excellence & API Support Leader Sligo Not Disclosed
Research and Development Compliance Specialist Galway Not Disclosed
QA Manager Biologics Dublin West €70000 - €80000
Quality Manager Combination Products Dublin Not Disclosed

Process Development Engineer Career Profile

Process Development Engineer

A Process Development Engineer or New Product Introduction Engineers is charged with taking a concept or a prototype from small scale into full scale commercialisation. Process Development Engineers require a strong project management background as the role is cross functional and requires interaction with many different groups, R&D, Quality, Manufacturing, Reg Affairs etc Very often role will require international travel as R&D facility may be located in a different country to manufacturing facility

Typically the Process Development Engineer will have a degree in Engineering and 2-3 years experience in scales up, tech transfers and commercialisation projects. Good communication skills are essential.

Key Responsibilities of the Process Development Engineer


  • Co-ordinating all activities to design, develop and introduce to production new products in accordance with the requirements of ISO 13485:2003 & latest Medical Device Directive & other standards that may apply.
  • Co-ordinating the generation of Design Files, Technical Files and Project Files to include Design Objectives, Design Reviews, Design Outputs, Design Verifications, Shelf Life studies, Bio-compatibility, Sterilisation, Risk Analysis, Validation Master Plans, IQ's, OQ's, PQ's, Test regimes etc., as required for new products and significant changes in existing products.
  • Co-ordinating the activities required to develop new products and processes.
  • Co-ordinating the acquisition of new materials required for new products
  • Co-ordinating the acquisition of new equipment and tooling required for new products, including test and measurement equipment.
  • Supporting the Business Acquisition process in providing technical support, drawings/specifications, samples, costing data and other information that may be required to generate new business.
  • Supporting the production department, especially with regard to new products, with regard to process issues, CAPA's, Engineering Changes, Customer complaints etc as and when required.
  • Ensuring all activities are carried out according to the relevant Medical and Industry standards and internal procedures.
  • Provide accurate and up-to-date reporting on projects





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