Senior Lead Manufacturing Engineer

Overview

Celestica Galway, Ireland is hiring a Senior Lead Engineer, Manufacturing Process Engineer to work on delivering a fully automated high-volume manufacturing line from development to full-scale production ramp for medical devices in a dynamic, fast-moving environment within the Automated Technology Solutions & Health-tech (Medical Device) market.

A career at Celestica is 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.

Your next challenge will be…

Design, develop, deploy and optimize manufacturing processes to achieve quality, cost and delivery goals for Celestica and its customers. Provide ongoing support to a complex high-speed automated production line and new product introductions. Support a product family in the ATS & Medical Device markets, collaborating with operations, technical and quality teams and product designers to drive projects that improve line performance and contribute to new business opportunities. The role reports to the Engineering Manager.

Your day-to-day activities

• Understand and implement the customer's technical roadmap and related process development projects.
• Lead and implement the development and release of the full manufacturing process for new customer products.
• Understand and provide feedback on customer technical requirements to team members and management.
• Develop and implement costed, optimized feedback using Design for Manufacturability (DFX) tools and processes to reduce manufacturing cost and improve quality and reliability.
• Develop, plan and lead assessment of process capability using the design of experiments.
• Devising process controls and data collection strategies; evaluate complex data to report yield, reliability and identify root causes of failures impacting product quality.
• Project Management: manage/lead complex, multi-line engineering projects, coordinating with other functions; create and execute project/change management plans within time and budget; identify barriers and mitigation plans.
• Financial acumen and business planning: create financial plans, profitability calculations, risk analyses, and ensure alignment with internal/external reporting requirements relevant to your area.
• Coaching/Mentoring; Communication/Negotiation/Presentation; Creative Problem Solving; Stakeholder Management; Quality & Lean; DOE; D/PFMEA; 8D/Corrective Action; Equipment Safety.
• NP I-PCBA and DFX activities spanning ESD, component prep, soldering processes, assembly, testing, data analytics and related manufacturing operations.
• Other related competencies as required to support the manufacturing line and product introductions.

What do we offer?

• Market-competitive total rewards: flexible salary with fixed and variable components based on goals.
• Opportunity to be a key member of the new product introduction team within Health Tech Engineering, driven by innovation.
• Training and development opportunities to support growth and career advancement.
• Opportunities to innovate, mentor others and realize your own career vision.
• A global, collaborative culture with leadership that supports your growth and professional opportunities.

What do we expect from you?

• Excellent Project Management and Time Management skills.
• Experience creating CAPA, FMEA, SOPs, Control Plans and performing validation (FAT, SAT, IQ, OQ, PQ).
• Ability to effectively communicate manufacturing plans, proposals, results, and negotiate options at management levels.
• Strong analytical and problem-solving skills.
• Excellent interpersonal and communication skills.
• Strong report writing and data analytics capabilities.
• Knowledge of the medical device industry and of regulatory frameworks (e.g., 21 CFR, ISO particularly in Change Control and Validation is advantageous.

What are we looking for?

• A Degree in Engineering with 4+ years of relevant experience.
• Relevant Medical Device and/or Automation experience preferred.
• Experience in ISO 13485 medical device manufacturing environment is desirable.
• Strong project management experience with NPI knowledge.
• Ability to initiate and lead change, collaborate, drive accountability, think critically and make sound decisions.
• Open to short-term travel assignments, particularly early in projects.
• Excellent customer management skills and knowledge of customer and regulatory requirements.
• Experience coaching and mentoring junior engineers.

Equal Opportunity

Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).

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