I'm looking for...

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

Google Chrome
Internet Explorer
Mozilla Firefox

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Contact Info
Quality Engineer
Dublin South
QA Manager
Dublin City Centre
SAP Planner
QC Manager
QA Manager
R&D Engineer
API Purchaser
Project Engineer
Dublin North
Snr QA Specialist
Dublin South
Quality Assurance Manager
Republic of Ireland
R&D Engineer
QA Manager Biologics
Dublin West
Program Manager
QA Manager
Dublin West
Administration Support
Dublin North
Supply Chain Analyst
Dublin North
Risk Manager
QA Manager
Dublin North
National Sales Representative
Republic of Ireland
Apply for this job






Salary Expectations:



Current Location:

Notice Period:

Write here your cover note:

If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to applications@lifescience.ie

Project Engineer

Reference:SGATBE-516061 Location: Dublin
Qualification:DegreeExperience:4-5 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: EHS Engineer, Project Engineer

Project Manager – Medical Device

Life Science Recruitment are looking for a Project Manager (PM) with a Biomedical or Mechanical Engineering background to coordinate product development projects on our clients Drug Delivery platform, between teams in Ireland and the UK. The successful candidate will have excellent interpersonal and organisation skills and be fluent in English, allowing them to coordinate the activities of teams across multiple sites to deliver new projects. Prior experience in project management is essential for consideration.

Roles & Responsibilities

• Project planning to deliver project(s) against agreed milestones and project scope (schedule, resource, cost).
• Scheduling and driving project meetings.
• Allocating tasks and deadlines.
• Regular reporting on the project status, performance and risks to the Programme Manager.
• Ensuring requirements and specifications are well defined.
• Integration of documentation into and maintenance of the design history file.
• Facilitation of good communication between cross-functional teams in Ireland and the UK with key stakeholders, external partners and vendors to deliver project goals.
• Short term production and supply chain management (Cleanroom) Generation and updates to Bills of Material.
• Raise and manage engineering change documentation.
• Create and modify Quality System documents.
• Liaise with existing or new suppliers (request for quotes, manufacture of parts etc).
• Planning and execution of verification and validation activities, including assisting in the generation of Validation Master Plans.
• Assist with the planning/execution of Equipment Validations (IQs/OQs) and subsequently Design Verification and Process Validation (OQ / PQs).
• Support Regulatory Affairs with product submissions.

Skills & Qualifications

• Third level degree in Mechanical, Manufacturing or Production Engineering or similar discipline. Minimum of three years in product / process development, ideally in Class II / III medical devices in addition to two years minimum in a project management capacity.
• Strong interpersonal and team skills with ability to collaborate effectively and demonstrate conflict resolution.
• Solid planning and organization skills including attention to detail, multi-tasking, critical thinking and problem-solving skills.
• Skilled in preparing documentation such as project plans, schedules / timelines, checklists, protocols, and reports that are often detailed and complex.
• Comprehension of development/engineering principles, sufficient to allow participation in new product development or other projects. Although not essential, it is desirable if applicants have the following:
• Certification from an accredited institution in Project/Program Management.
• Knowledge of medical device quality & regulatory systems and medical device directive (ISO13485, MDD and FDA CFR 820) and other pertinent Design Control requirements.
• Knowledge of anatomy and physiology.
• Knowledge of manufacturing processes within a clean-room environment.

If you would like further Information you can contact the recruiter directly:

Simon Gillivan | Tel: +353 (0) 1 507 9258