We are currently partnering with our medical device client in Galway who are looking to hire a Global Technical Project Manager to join their team. This role can be worked on a hybrid model.Job Purpose:The Technical Project Manager will lead the operations portion of new product development, site transfers, acquisition integrations, and other manufacturing projects for Sourced Finished Medical Device (SFMD) products.The role is responsible for ensuring the seamless execution of projects of varying sizes, from small tasks to large programs, working with external manufacturing partners. The PM will manage multiple projects simultaneously, guiding cross-functional teams.Key Responsibilities:Lead cross-functional teams from internal and supplier resources, providing technical guidance.Assemble and coordinate resources to drive project completion.Prioritize tasks based on business needs, timing, and financial risk.Ensure manufacturability of transferred products using best practices and tools.Proactively identify and resolve issues affecting quality, cost, or service levels.Create project tracking plans, schedules, and risk assessments.Delegate tasks based on team skills and project risks, removing barriers to progress.Serve as a technical resource for supplier initiatives, including Change Notifications.Resolve conflicts and engage functional management to ensure timely completion.Present project updates to upper management and stakeholders as needed.Education & ExperienceMinimum Qualifications:7+ years of engineering experience (manufacturing, process development, or related).Bachelor’s degree (240 credits), preferably in engineering.Strong organizational and execution skills with the ability to lead projects.Ability to travel up to 25% domestically and internationally.Preferred Qualifications:3+ years of project management experience in Operations or Development.Experience working with external suppliers or as a supplier to large customers.Medical device manufacturing experience, including equipment qualification and process validation.Familiarity with continuous improvement projects.Experience in manufacturing production transfers.Knowledge of regulatory standards and internal SOPs is a plus.PMP certification is a plus.For a confidential discussion, a more detailed job spec and more information on the role, please contact Amy Newell.amy.newell@collinsmcnicholas.ie091-706718
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