Senior Process Development Engineer – Galway

Senior Process Development Engineer – Galway
Fantastic opportunity to join a well known Medical Device company in Galway as a Senior Process Development Engineer with great benefits and opportunities for progression

Key Responsibilities
  • Provides Technical Leadership to Engineers and technicians within own team and to wider Stakeholders to provide direction on optimum solution(s) to the Process Development of new Moulded, Extruded and Balloons Components. 
  • Provide scientific understanding and technical engineering skills to meet business goals and objectives.  Ability to coach, lead and enhance the productivity of technical reports within the business.   Provide a structured framework for training of technical reports.  Build collaborative relationships through strong teamwork across the organization.
  • Initiates cross-functional partnerships to identify and resolve process related issues.
  • Provides Technical Leadership in the selection, design, optimisation, validation and troubleshooting, of key processes & product technologies.
  • Leads the development and execution of experimentation and testing to enable characterisation, optimization and troubleshooting of key processes and equipment.  Summarises, analyses, and draws conclusions from test results leading to effective technical resolution.
  • Facilitates the use of Six Sigma & Problem-Solving tools leading a team of engineers and technicians in the characterization, optimization and troubleshooting of process equipment and technology performance.
  • Liaises with Equipment Engineering or external equipment/tooling or material vendors in the selection, design & development of new (or upgrades to existing) equipment, tooling and materials.
  • Co-ordinates the introduction of new processes, equipment and materials including installation, calibration, EHS assessment debug, and all associated process and quality system documentation requirements including technical and process work instructions.
  • Demonstrates strong knowledge and application of Process and equipment validation techniques, PFMEA’s/PRA’s and associated regulatory requirements and applies this knowledge in the efficient & timely validation of equipment and processes.
  • Leads the writing and release of process validation documentation including PFMEA/PRAs, Validation Plans, protocols and reports.
  • Leads execution and documentation of validation builds, co-ordinates testing of validation units and the compilation, analysis and reporting of the validation results.




Skills Experience & Qualifications
  • A seasoned, experienced professional with a complete understanding and wide application of principle, theories, and concepts in the field.
  • Has a minimum of 5 years’ experience in Polymer component Manufacture in a Medical Device Industry.
  • Ideally is Qualified in Polymer Engineering/Science or equivalent (Level 8 or higher).
  • General knowledge of other related disciplines, business unit function and cross group dependencies/relationships.
  • This job is the fully qualified career-oriented position.

If you would like to know more, please reach out to me on vincentkenny@cregg.ie or 061 363318

Apply for this job

Job Details

23 February 2024
Job ID: 9175

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