Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevents future issue
Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.
What You Will do:
Risk Management
Proficient in risk management practices and tools, having high expertise in failure modes associated with production and production related processes, (PFMEA).
Support the Risk Management File through risk Management Principles. Responsible for the evaluation of process risks, risk mitigation and ensures appropriate production and process controls are identified, qualified, and implemented throughout the product manufacturing lifecycle (at supplier, incoming of materials/components, manufacturing, until product release) through robust pFMEA.Ensure all Risk Management outputs comply with ISO 14971.Support Design team to complete CQA/CTQ identification and inputs to dFMEA to enable process risk identification, process characterization, process capability and robust process control.
Inspection
Develop and implement lean inspection strategies and inspection plans through state-of-the-art inspection methods and technologies. Ensure inspections are repeatable, efficient, and scalable.
Lead continuous improvements of inspection methods and sampling plans, with a focus on human error risk elimination
Validation
Support the development, execution, and approval of validation strategies, with the goal of highly capable processes, that result in high yield and enable scalability. Approve protocols and reports, including data analysis.
Influence processes towards validation versus manual verification, where possible.Support Sterilisation validation activity, as required
Process Excellence
Apply appropriate statistical techniques to ensure the development of robust, predictive quality systems which are easily transferable and maintainable in a production environment.
Provide expertise for NC’s & CAPA’s related to new products. Act as a subject matter expert and mentor in problem solving and root causing tools.
Support Design for Manufacture and Assembly (DFMA) through process design, inspection optimization, application of state-of-the-art technologies and tooling & fixture development.
Purchasing Controls
Lead the supplier qualification strategy and approve the supplier validations and Production Part Approval Process (PPAP). Ensure Supplier’s Quality Systems can complete process characterization and develop highly capable processes that are scalable, and meet Stryker expectations.
Provide Quality input to influence the proper selection of suppliers.Support implementation of supplier certification.Support Supplier Quality to establish Quality Agreements with Stryker sites and suppliers as part of NPI projects.
Design Transfer
Represent quality assurance during the DTAP (Design Transfer Agreement Plan) process, ensuring product launches meet or exceed established metric targets including supplier DPM, right first time, manufacturing loss, manufacturing complaints per million, units recalled, product escapes and use-as-is, in conjunction with other targets per the DTAP. Represent NPI Quality Assurance at Design reviews and ensure integrity of the process design through robust NPI quality deliverable
Provide subject matter expertise in Design transfer processes and procedures, participating and interfacing in internal & external audits with regulatory representatives.
What You Need:
Must have
Bachelor of Science, Engineering or related subject in Electrical/Electronics/Mechanical with 5 years’ experience in APQP, New Product development, PPAP and Design Transfers.
Analytical & problem solving skills, process improvement orientation, and the ability to handle multiple tasks.
Competency in Metrology including ability to interpret complex engineering drawings and understand geometrical dimensioning and tolerance. Knowledge in selection & development of inspection techniques – automated inspection techniques such as CMM and vision systems a plus.
Working knowledge/experience of risk based and statistical techniques, in particular process risk, failure mode and effect analysis (FMEA), statistical sampling plans, process capability and MSA’s.
Preferred
Previous experience in a regulated environment within a manufacturing environment required (medical device, pharma, aerospace, automotive). Atleast 4 years’ experience in new product/process and/or supplier quality is desired.
Candidate working on OEM NPI Team would be desirable. ASQ CQE, CSQP or equivalent course work / experience desirable
Proficient in understanding of Medical Device manufacturing processes desirable.Familiarity with ISO 13485, QSR, GDP, GMP desirable.
Lean Six Sigma training has a distinct advantage.Highly proficient in all aspects of Validation. Computer System validation will be a distinct advantage.
Experience in executing complex problem-solving and process improvements techniques related to design/process/technical issues using lean six sigma tools like DMAIC.
