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.
Job Description:
You will have the opportunity to work on delivering a fully automated high volume manufacturing line from development stage to full scale production ramp producing world class medical devices in a dynamic, fast moving environment.
Your responsibilities will include leading validation activities, process/procedure definition and maintaining a continuous flow of high quality products to our customers in a medical device environment.
This position will be responsible for supporting some of our product family in the Med tech sector liaising with Production, Engineering, Supply Chain and Customer contracts reporting into our Quality Manager.
Your day to day activities will include:
* Providing expert QE technical direction/input to qualification and validation activities in conjunction with Design, Engineering and extended QA teams.
* Authoring and supporting (input and critical review) of qualification/validation protocols/reports.
* Leading the team to handle all quality excursions independently, and taking effective actions on time.
* Overseeing the product ramp; material quality from NPI to mass production.
* Developing the quality control plan for respective area (material/process/product).
* Monitoring and reporting quality KPI for internal (factory) and external (customer).
* Driving continuous improvement to benefit customer, CLS and supplier.
* Developing and maintaining internal quality system, procedures, work instructions and standards.
* Coaching / mentoring staff members on quality topics to improve quality knowledge.
* Supporting the team and the organisational priorities in the quality deployment strategy.
* Working with supplier Engineering and helping to address supplier quality issues.
* Taking quality technical ownership for PFMEAs in conjunction with process engineering.
* Analysing data and providing real time feedback to ensure all manufacturing and process defects are detected and eliminated.
What 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.
* Quality 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.
Requirements:
* A minimum of 4+ years Quality engineering experience is preferable.
* Some materials engineering experience or quality materials testing knowledge is an advantage.
* Someone with Med-tech experience.
* Someone with an ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically and make sound decisions.
* Experience of 6 Sigma quality methods would be a distinct advantage.
* Someone with a level 8 degree (240 credits) or equivalent in an Engineering or Science related discipline.
* However, postgraduate qualifications etc. will be considered if supported with relevant experience.
* Someone that is open to the opportunity of short term travel assignments particularly at the early stages of the project.