Senior Lead Engineer, Manufacturing Process

Req ID: 122990 
Remote Position: No
Region: Europe 
Country: Ireland 
State/Province: Galway 
City:  Galway 

Your next challenge will be…

To become responsible for designing, developing, deploying and optimizing processes for manufacturing to achieve quality, cost and delivery goals for Celestica and its customer’s products. This role provides support and ongoing development to a complex high speed automated production line and new product introductions. This position will be responsible for supporting some of our product family in the ATS & Medical Device markets working closely with the operations, technical and quality teams and product designers to drive projects that continually improve the line performance as well as solution and provide input to new business opportunities. The position will report into our Engineering Manager.

Your day to day activities will include the following…

• Being responsible for understanding and implementing the customer’s technical roadmap and related process development projects;
• Leading and implementing the development and release of the full manufacturing process for new customer products;
• Understanding and providing feedback on customer’s technical requirements to team members and management;
• Developing and implementing costed and optimized feedback using Design for manufacturability (DFX) tools and processes, with the goal of reducing manufacturing cost and improving quality and reliability of product;
• Developing, planning and leading the assessment of the capability of process applications using the design of experiments;        
• Devising process controls and data collection strategies and evaluating complex data to assist with reporting yield, reliability and diagnoses to root causes failures impacting product quality.

What do we expect from you?   

• Excellent Project Management and Time Management skills;
• Excellent communication Skills both written and verbal;
• Knowledge in performing validation (FAT, SAT, IQ, OQ, PQ);
• Creative Problem Solving; Customer Interaction/Stakeholder Management; Quality & Lean; Working Effectively with Others; D/PFMEA; 8D/Corrective Action; Equipment Safety; Design of Experiments (DOE);
• Ability to effectively communicate manufacturing plans, proposals, results, and negotiate options at management levels;
• Strong analytical and problem solving skills;
• Excellent interpersonal & communication skills;
• Strong report writing, presentation & data analytical capabilities;
• Advantageous to have knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation;
• Strong people leadership skills.

 What are we looking for?

• Someone with a Degree in Engineering with 5+ years' relevant experience;
• Relevant Medical Device AND/OR Automation experience preferred;
• Experience in ISO13485 medical device manufacturing environment is desirable;
• Relevant project management experience and associated qualifications with NPI experience;
• Someone with an ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically and make sound decisions;
• Someone that is open to the opportunity of short term travel assignments particularly at the early stages of the project;
• Someone that has excellent customer Management skills and a knowledge of customer and regulatory requirements;
• Someone that has previous experience of coaching and mentoring junior engineers.

What do we offer?

• Market-competitive total reward: flexible salary, fix and variable salary based on goals
• The opportunity to become a key member of the new product introduction team in the Health Tech. Engineering function driven by innovation where creativity matters.
• Training and development opportunities, with us the sky is the limit!
• The opportunity to innovate, learn, mentor others and work toward your own vision of career success
• A global, collaborative culture with strong leadership imperatives to foster your growth and  

          professional opportunities

• A sustainable culture where we provide opportunities for employees to give back to the community

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).

At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

COMPANY OVERVIEW:

Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud.

Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.

Celestica would like to thank all applicants, however, only qualified applicants will be contacted.

Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.