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Project Engineer

ID
14491
Location
Castlerea
Role Type
Permanent

Project Engineer

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Job Title: Project Engineer

Reporting to: Business Unit Engineering Manager

Overview:

We are working with a client who are based in Roscommon and they are seeking a Project Engineer with a robust understanding of engineering principles, theories, concepts, practices, and techniques.

This role involves providing manufacturing support, spearheading process improvement initiatives, and managing projects across various product lines.

Essential Duties and Responsibilities

Manufacturing Support:

  • Provide support across a range of manufacturing processes to ensure smooth operations.
  • Lead and implement process improvement initiatives aimed at reducing costs and improving manufacturing efficiency using data analysis.

Project Management:

  • Manage projects from conception to completion, including new product introduction and process implementation.
  • Conduct process and product validations to ensure compliance and quality.
  • Implement product, process, and material changes through validation, change control, and documentation updates.

Cross-functional Collaboration:

  • Work across various product lines, familiarizing yourself with different processes to provide versatile support.
  • Collaborate with cross-functional teams including quality, production, and supply chain to achieve project goals.

Compliance and Documentation:

  • Adhere to the requirements of the quality and environmental management system.
  • Ensure all work is guided by due diligence and compliance, maintaining high standards in all aspects of the job.
  • Maintain and update relevant documentation to reflect changes and improvements.

Additional Responsibilities:

  • Perform additional ad hoc duties and projects as assigned by the Engineering Manager.

Qualifications and Experience

Required:

  • Level 8 or equivalent degree in Engineering or a related discipline.
  • At least 3 years of experience in a medical device manufacturing engineering role.
  • Knowledge and experience with medical device validation protocols and associated documentation.
  • Strong background in process engineering with practical experience in implementing validation protocols.
  • Familiarity with ISO 9001:2008 and ISO 13485 standards.
  • Proficiency in MS Office applications.

Desirable:

Experience with AutoCAD and SolidWorks.
Knowledge of Lean and Six Sigma methodologies.
Experience with new product introductions.
Strong team player with the ability to work independently.
Excellent interpersonal skills and the ability to collaborate with cross-functional teams.
Ability to plan, organize, and prioritize tasks to meet deadlines

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

 

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