**What you will do:** ** ** + Ensuring compliancetoSupplier Control activitiesidentifiedbyorganization. + Experience of PPAP associated with New Product Launches and Management of Production cycles there after (Manufacturing Transfers). + Participate in cross- functionalteams in the development of new products or changes related to current products in meeting customer requirements. + Applies sound, systematic problem-solving methodologies (5Why, DMAIC, 8D, C&E) inidentifying, prioritizing, communicating, and resolving quality issues - NC & CAPA tofacilitateroot cause analysis and corrective actions of supplier quality issues. + Promote the use of continuous improvement methodologies such as Lean, Six Sigma,Poka- Yoke (Error Proofing), Measurement System Analysis (MSA), Statistical process control (SPC) and Process Failure Mode and Effects Analysis (pFMEA) + Evaluate Quality data toidentifyprocess improvement opportunities within the supply chain. + Coordinate Change Management & Control with Suppliers and implement changes at Supplier. + Review of process and equipment Validation including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Special Process Validations, and Test Method Validations. + Inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met. + Prioritizing, reviewing, and delivering First Article Inspections FAIs for sustaining parts and development projects.   **What you need:** ** **   **Required:** ** ** + B.Tech(Electronics/Electrical/Mechanical) with 2-5 years of experience in Quality / Engineering / Manufacturing environment. + Quality Processes/ Tools - Working knowledge of basic and advanced Quality tools suchas;PPAP, Six Sigma, SPC, FMEA, Control Plans, Root Cause Analysis, Poke Yoke, Kaizen, Lean Manufacturing etc. + Executes/implements/ improve all supplier quality tools/ Processes. Trainssupplierin these tools effectively. + Proficient in MS Office Suite (including Word, Excel, Power Pointetc). + Strong interpersonal skills to work with cross-functional teams (engineering, R&D, manufacturing, regulatory affairs). **Preferred:** ** ** + Understanding of Medical Device Regulatory Compliance (ISO 13485, CFR 820, or comparable standard / regulation) and EU's Medical Device Directive. + Excellent communication and influencing skills, with the ability to manage multiple tasks and represent the Quality function across teams + Preferred ASQ Certified Quality Engineer (CQE) **.** + Commodity Domain Knowledge – Strong Knowledge & understands technology, regulatoryrequirementrelated to product, system & services.  + Proventrack recordof leading successful process implementation projects Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.