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James Cassidy
Life Science

+353 1 5079250
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Technical Project Manager

Reference:JC/HQ00001455 Location: Westmeath
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed

Technical Project Manager

Our client a medical device multinational currently seeks a technical project manager to join their team. Reporting to Team Leader Materials Development and Rationalization Team. The successful candidate will lead, coordinate and provide, within a dedicated project driven strategy, all technical phases of design change, whether in product development or product reengineering, including design and development planning, develop product performance specification and requirements definition, product development process, evaluation and manufacturing aspects using design control and Product-to-Market Processes.
Ideal Candidate for this position is an optimistic self-starter that is results driven, who excels in a dedicated or project focused, transparent, and team based environment.

Engineering lead for all aspects of re-engineering existing products including the design, prototyping, testing (verification and validation), risk management and documentation. Lead the redesign of existing components to improve quality, utilize automated product techniques, optimize process capabilities, and produce better products in a more cost-effective manner.
Interface with clinicians, marketing, and process development to understand customer preferences/requirements and establish design criteria for new products and product improvements.
Identify and create new design and/or process concepts. Design and validate products and components using engineering principles and adhere to the design control process as appropriate.
Lead, conduct and/or participate in design and technical phase reviews.
Interface with vendors to obtain quotations, purchase components, and debug problems with production parts.
Interface with Sourcing to develop vendor supply agreements for components and/or new products.
Interface with process development engineers, manufacturing and lab technicians to design and develop new fixtures, tooling, and machinery. Assist in the development and qualifications of required manufacturing processes.
Assist process development and manufacturing personnel with the transfer of development projects and design changes into production.
Support regulatory submissions and clinical trials as required.
Update and review project progress on an as required basis by supervisor.
Meet all project objectives, milestones, and target dates.
Assist in the tracking and communication of project developments from prototype design through testing and into production. Formulate decisions to facilitate project advancement.
Ensure projects are developed and documented compliant to the Quality System.
Adhere to and ensure the compliance of Code of Ethics, all Company policies, rules, procedures and housekeeping standards.
Skills / Experience
BS – Engineering displine or disipline or Professional Engineer (PE) certification
Preferred Engineering fields:BioMedical, Mechnical, Electronic, Packaging, Plastics, Industrial
1-5 years experience in a project engineering role
2 years in medical device preferred
Strong analytical and problem-solving skills
Team player with good interpersonal skills
Specialised Skills & Oher Requirements
Proficent in Microsoft Office Suite, including Project, and computerized analysis applications
CAAD (design/drafting) or SolidWorks for part design and review
Lean and/or Six Sigma Certification/Training/Exposure
Working knownledge of the following manufacturing processes and methods:
PCB/PCBA/Box Build

James Cassidy | Tel: +353 (0) 1 5079250