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Senior Project Manager

  • On-site
    • Wicklow, Ireland
  • Engineering (Continuous Improvement / Lean / Projects)

Job description

A rapidly expanding medical device manufacturer is seeking a Project Engineer II / Senior Project Engineer to join its high-performing team in Wicklow. This is a key engineering role focused on supporting new and existing manufacturing projects in a fast-paced, regulated environment.

The successful candidate will have strong project management skills, excellent communication abilities, and a proven track record within medical device manufacturing. This is an exciting opportunity to contribute to innovative product development and process improvement initiatives, with a focus on plastics and injection moulding.

Responsibilities include but are not limited to:

  • Lead and support technical projects from concept through to validation and implementation on the manufacturing floor.

  • Collaborate with cross-functional teams including Engineering, Quality, and Operations to execute project plans.

  • Manage timelines, resources, and documentation to ensure projects are delivered on time and within scope.

  • Interface with customers and external suppliers to ensure alignment with project requirements and manufacturing standards.

  • Support process validation activities (IQ/OQ/PQ) in line with regulatory and quality expectations.

  • Drive continuous improvement and problem-solving initiatives across processes and systems.

  • Provide technical input on equipment selection, tooling design, and manufacturing methods.

  • Ensure all project documentation, reports, and protocols meet internal and external standards.

Job requirements

  • Degree in Engineering – Mechanical, Manufacturing, Process, or Biomedical preferred.

  • Minimum of 4–5 years’ experience in a regulated medical device manufacturing environment (MNC or contract manufacturing).

  • Demonstrated experience managing engineering or process development projects.

  • Strong written and verbal communication skills — able to clearly present ideas, timelines, and technical information.

  • Experience in injection moulding, tooling, and plastics manufacturing techniques.

  • Solid knowledge of process validation practices and quality system requirements.

  • Proficiency with Microsoft Office, including MS Project; knowledge of Minitab or equivalent is an advantage.

  • Familiarity with CE Marking, GDP, and Lean/6 Sigma methodologies is desirable.

Immediate interviews available for suitable candidates

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other relevant STEM roles.

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