Senior Quality Engineer 1

at  Celestica

SUMMARY

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.
By Joining Celestica Galway (Ireland) as a Senior Quality Engineer you will have the opportunity to work with incredible team taking on the amazing challenge of becoming an emerging leader in the introduction of new Medical Device products. You will become responsible for dealing with the three major phases of Quality Management, Quality Planning/Prevention, Corrective Action.
Your next challenge will be…
Lead process/procedure definition and maintain a continuous flow of high-quality products to our customers in a contract manufacturing environment including regulatory content for the latest and more innovative medical devices. This position will be responsible for supporting some of our product family in both the Med tech and Industrial sectors liaising with Production, Engineering, Supply Chain and Customer contracts reporting into our Quality Manager.

DETAILED DESCRIPTION

Your day- to-day activities will include:
Mentors and develop personnel in the practices of Quality management and Quality improvement
Lead the team to investigate any quality excursions and implement corrections and corrective actions
Manage performance of reports
Lead the quality group in a fast-paced production environment
Customer liaison for quality escalations and daily quality issues ensuring measured, developed and timely responses to the customer.
Support the change management process and Customer requests as appropriate.
High level of competence using relevant corrective action systems (e.g CAPA)
Create concise and accurate technical reports, communicate results and manage subsequent analysis queries
Continually seek to drive improvements in product and process quality.
Create and evaluate metrics to drive the quality improvement processes.
Own, Maintain and report timely and accurate KPI’s
Manage and maintain the NCMR database and report weekly to the customer.
Using appropriate statistical techniques to monitor process performance (e.g.SPC, Minitab, Ppk, Gage R & R analysis, sampling techniques).
Provide quality engineering support to the facility, including validation and risk management and review of technical documentation (eg. FMEA’s, control plans).
Ability to design tests, evaluate results and recommend solutions to improve the processes associated with our manufacturing.
Support the development of test processes, test fixtures and specialised tools to automate test development.
Apply project management skills and methodology as necessary for key CI projects.

KNOWLEDGE/SKILLS/COMPETENCIES

What do we expect from you?
Ability to effectively lead, manage, train and motivate employees
Strong knowledge of quality tools, ISO / QMS standards and processes (ISO 9001, ISO13485)
Knowledge of data analysis and presentation software and its uses in generating reports, capturing data and presenting data in an understandable format.
Strong knowledge of product and manufacturing processes and materials properties
Knowledge and understanding of the manufacturing environment and how decisions impact customer satisfaction product quality, on-time delivery and profitability of the unit
Knowledge of quality tools such as FMEA, PMP, SPC, 8D methodology, etc.
Knowledge of Six sigma and Lean Kaizen.
Ability to effectively communicate with a wide variety of internal and external customers to summarize complex technical issues
Knowledge of Med-tech and regulatory requirements (such as FDA and MDR) is a requirement of the role with
pharma & food safety systems an advantage
Ability to effectively lead and manage several projects simultaneously and coordinate multiple, changing deadlines while also working effectively on their own and in a team environment.
Ability to be an Internal Auditor
What are we looking for?
Bachelor’s degree in related field
6 years or more experience in a manufacturing environment within a Quality function
Experience in a Med-tech environment is essential
Experience of 6 Sigma quality methods would be a distinct advantage.
Materials engineering experience/quality materials testing knowledge is an advantage
Experience of leading a team is an advantage.

NOTES

This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.
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.

Please refer the Job description for details