Process Engineer

Roscommon - Ireland

Monthly Salary: Not Disclosed

Experience Required: 4-5years

Posted on: 14 hours ago

Vacancies: 1 Vacancy

Job Summary

ID Recruitment are working with a large medical device manufacturing company in Roscommon to recruit a Process Engineer.

The role which will join with a team of process engineers will work within the manufacturing team responsible for driving continuous improvement supporting day-to-day operations and delivering waste elimination initiatives. This role will interface directly with customers on product development and complaint investigations while also supporting the introduction of new technologies and processes. Operating in a fast-paced quick-turnaround environment the Process Engineer will ensure robust efficient and compliant manufacturing processes that meet internal and external expectations

Role and Responsibilities

The ideal candidate has experience in successfully leading x-functional problem-solving teams with the skills necessary to seek out and eliminate waste. You will liaise with quality sales customers and suppliers regarding technical production issues.
Act as the technical lead for assigned production areas supporting delivery of key performance metrics including yield uptime and quality.
Lead and support CI initiatives focused on waste elimination cost reduction and process optimization using Lean and Six Sigma methodologies.
Own and drive structured investigations into customer complaints and internal non-conformances ensuring timely root cause analysis and effective CAPA implementation.
Collaborate with cross-functional teams to introduce and validate new equipment technologies and processes.
Provide technical support for the transfer and scale-up of new products into manufacturing including documentation training and process readiness.
Maintain strong communication with customers suppliers and internal stakeholders to resolve technical issues and support development activities.
Champion a hands-on data-driven approach to problem solving and process improvement.
Ensure compliance with quality system requirements GMP 6S and safety standards.
Support training and development of operators and technicians to build technical capability across the team.
Maintain effective documentation and reporting in line with site and divisional standards.

Requirements

Bachelors degree in Polymer Mechanical Manufacturing Engineering or related discipline.
Minimum 3 years experience in a manufacturing/process engineering role ideally within the medical device or regulated industry.
Proven experience in process improvement waste elimination and structured problem solving.
Hands-on experience with extrusion or polymer processing is a strong advantage.
Familiarity with ISO 13485 FDA and quality system requirements.
Lean Six Sigma Green Belt or higher preferred.
Project Management skills.
Communication skills verbal written and presentation.
Good statistical and data analysis knowledge (minitab experience is beneficial).
A high degree of flexibility in a continuously changing environment.

Required Skills:

Bachelors degree in Polymer Mechanical Manufacturing Engineering or related discipline. Minimum 3 years experience in a manufacturing/process engineering role ideally within the medical device or regulated industry. Proven experience in process improvement waste elimination and structured problem solving. Hands-on experience with extrusion or polymer processing is a strong advantage. Familiarity with ISO 13485 FDA and quality system requirements. Lean Six Sigma Green Belt or higher preferred. Project Management skills. Communication skills verbal written and presentation. Good statistical and data analysis knowledge (minitab experience is beneficial). A high degree of flexibility in a continuously changing environment.

ID Recruitment are working with a large medical device manufacturing company in Roscommon to recruit a Process Engineer.The role which will join with a team of process engineers will work within the manufacturing team responsible for driving continuous improvement supporting day-to-day operations an...

ID Recruitment are working with a large medical device manufacturing company in Roscommon to recruit a Process Engineer.

Role and Responsibilities

The ideal candidate has experience in successfully leading x-functional problem-solving teams with the skills necessary to seek out and eliminate waste. You will liaise with quality sales customers and suppliers regarding technical production issues.
Act as the technical lead for assigned production areas supporting delivery of key performance metrics including yield uptime and quality.
Lead and support CI initiatives focused on waste elimination cost reduction and process optimization using Lean and Six Sigma methodologies.
Own and drive structured investigations into customer complaints and internal non-conformances ensuring timely root cause analysis and effective CAPA implementation.
Collaborate with cross-functional teams to introduce and validate new equipment technologies and processes.
Provide technical support for the transfer and scale-up of new products into manufacturing including documentation training and process readiness.
Maintain strong communication with customers suppliers and internal stakeholders to resolve technical issues and support development activities.
Champion a hands-on data-driven approach to problem solving and process improvement.
Ensure compliance with quality system requirements GMP 6S and safety standards.
Support training and development of operators and technicians to build technical capability across the team.
Maintain effective documentation and reporting in line with site and divisional standards.

Requirements

Bachelors degree in Polymer Mechanical Manufacturing Engineering or related discipline.
Minimum 3 years experience in a manufacturing/process engineering role ideally within the medical device or regulated industry.
Proven experience in process improvement waste elimination and structured problem solving.
Hands-on experience with extrusion or polymer processing is a strong advantage.
Familiarity with ISO 13485 FDA and quality system requirements.
Lean Six Sigma Green Belt or higher preferred.
Project Management skills.
Communication skills verbal written and presentation.
Good statistical and data analysis knowledge (minitab experience is beneficial).
A high degree of flexibility in a continuously changing environment.