Lead Manufacturing Engineer

A career at Celestica is only for those who want to do something extraordinary with a meaningful purpose: imagine, develop and deliver a better future with our customers.Celestica is a leader in high – reliability design, manufacturing and supply chain solutions that bring global expertise to every stage of product development.By joining Celestica Galway (Ireland) as a Lead Manufacturing Process Engineer, you will have the opportunity to lead the development and implementation of fully automated high-volume manufacturing lines from the development stage to full-scale production ramp, producing world-class medical devices in a dynamic, fast-moving environment.This position offers a great opportunity for a Lead Process Engineer to excel in a challenging environment of high-speed automation for micro assemblies across our business in the Automated Technology Solutions & Health-tech (Medical Device) market.Your next challenge will be...To lead and be accountable for process development, troubleshooting, and continuous improvement of the production process and equipment in the manufacturing area.This includes strategic planning and optimization of manufacturing processes.You will work closely with operations, technical & quality teams, and Product Designers to lead and drive complex projects that significantly improve line performance, provide innovative solutions, and contribute to new business opportunities.You will also be expected to mentor and guide other engineers within the team.This position will be responsible for leading the process engineering activities for one or more product families in the ATS & Medical Device markets, liaising with Production, Engineering, Supply Chain and Customer contracts, and reporting to our Engineering Manager.Your day-to-day activities will include the following...Oversee and analyze the performance of equipment, machines, and tools using advanced statistical methodologies to resolve complex equipment issues and optimize process parameters to eliminate non-conforming products, low yields, or product quality issues.Champion and drive continuous improvement processes for production areas using structured Process Capability and Lean Six Sigma methodologies, leading cross-functional teams in these initiatives.Create, execute, coordinate, and lead the design of experiments, test methods, protocols, specifications, and validation documentation (IQ/OQ/PQ) and oversee the development and execution of qualification trials/characterization studies.Manage multiple complex projects, generate comprehensive project plans, and lead project teams to drive completion and success, ensuring alignment with strategic objectives.Oversee the maintenance and calibration of critical equipment-systems, ensuring compliance and optimizing maintenance schedules.Interface with cross-functional teams and external vendors to integrate new products, processes, and technologies into the existing manufacturing area, leading the technology transfer and implementation.Lead the development of automated solutions for NPI programs, including new business development opportunities, and provide strategic input on automation strategies.Oversee and approve the qualification of engineering change management, ensuring robust change control processes.Mentor and provide technical guidance to other process engineers, fostering their development and growth.What do we offer?Market-competitive total reward: flexible salary, fix and variable salary based on goalsThe opportunity to lead new product introduction teams in the Health Tech sector.Engineering Function driven by innovation where creativity matters.Training and development opportunities; with us, the sky is the limitThe opportunity to innovate, learn, mentor others, and work toward your own vision of career successA global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunitiesA sustainable culture where we provide opportunities for employees to give back to the communityWhat do we expect from you?Extensive experience using engineering tools and software packages to design and automate complex manufacturing processes.Proven experience in detailed analysis, modeling, and methodologies to validate manufacturing process and tooling design and specifications.Extensive experience in creating CAPA, FMEA, SOP's, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ).Demonstrated ability to effectively communicate manufacturing plans, proposals, and results, and negotiate options at executive management levels.Exceptional analytical and problem-solving skills.Excellent interpersonal and communication skills.A strong aptitude for report writing and data analytics.In-depth knowledge of the medical device industry and of 21 CFR, (820, 11), ISO*****, specifically in the areas of Change Control and Validation.What are we looking for?A minimum of 4+ years' experience in a Process Engineering role, with a proven track record of leading projects and teams.A Primary Degree in an Engineering/Science discipline; a Master's degree is preferred.Medical Device AND/OR Automation experience is essential.Extensive experience in an ISO***** medical device manufacturing environment.Extensive experience in a highly automated manufacturing environment.A strong leader with the ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions.Someone who is open to the opportunity of short-term travel assignments, particularly at the early stages of the project.