Senior Quality Engineer
Acuity
Assembly
Senior Lead Engineer, Manufacturing Process
Celestica
full-time
Posted on:
Origin: • 🇮🇪 Ireland
Visit company websiteJob Level
Senior
Tech Stack
Assembly
About the role
- Design, develop, deploy and optimize manufacturing processes to achieve quality, cost and delivery goals for Celestica and customer products
- Support and provide ongoing development to complex high-speed automated production lines and new product introductions
- Support product family in ATS & Medical Device markets working closely with operations, technical and quality teams and product designers
- Drive projects that continually improve line performance and provide input to new business opportunities
- Lead and implement the development and release of the full manufacturing process for new customer products
- Understand and implement the customer’s technical roadmap and related process development projects; provide feedback on customer technical requirements
- Develop and implement costed and optimized feedback using Design for Manufacturability (DFX) tools and processes
- Develop, plan and lead capability assessments using Design of Experiments (DOE)
- Devise process controls and data collection strategies; evaluate complex data to report yield, reliability and diagnose root cause failures impacting product quality
- Report into the Engineering Manager and collaborate across cross-functional teams
Requirements
- Degree in Engineering with 4+ 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
- Excellent Project Management and Time Management skills
- Excellent communication skills, both written and verbal
- Experience creating CAPA, FMEA, SOP’s, 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 skills
- Strong report writing & data analytical capabilities
- Advantageous to have knowledge of the medical device industry and of 21 CFR (820, 11) and ISO13485, specifically in Change Control and Validation
- Ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically and make sound decisions
- Open to short term travel assignments particularly at early stages of projects
- Excellent customer management skills and knowledge of customer and regulatory requirements
- Previous experience coaching and mentoring junior engineers
- Enabling competencies may include: Coaching/Mentoring; Communication/Negotiation/Presentation; Creative Problem Solving; Customer Interaction/Stakeholder Management; Quality & Lean; Working Effectively with Others; D/PFMEA; 8D/Corrective Action; Equipment Safety; Design of Experiments (DOE)
- Technical competencies include extensive NPI-PCBA, DFX, FA LAB, Optical & XRay Inspection, Machining, Mechanical & Systems Assembly, Microelectronics skills listed in job posting
