What you will do: Implement sales activities to achieve budgeted sales and profitability goal for the assigned area / territory.Support Regional Sales Business Manager to promote products to individual doctors & hospitals in assigned region.Reach out to identify new business opportunities by means of tender & government businesses.Ensure efficient use of company's demo units in the territory.Collaborate & cooperate with ABM / ZSM as & when required.Retain key accounts & explore new accounts/business opportunities to build Strykers‘ customer poolIdentify, develop & manage different channels of business (distributors & direct sales) in the area.Provide solutions to customers to meet their specifications on the basis of techno-commercial discussions.Upgrade existing customers to newer technologies. What you need: Minimum 4-7 years’ sales experience in healthcare industry.Qualification must be Graduate /MBAMust have experience into Joint replacement segment.Location: Jaipur 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.

What you will do: Together with the software team, develop a testing strategy for testing during the developmental phase.Develop the verification and validation strategy/plan that meets the SDLC requirements within the project timeline and resource constraintsDevelop software test cases to verify the software requirements.Execute non-function testing which involves accuracy, reliability, performance.Execute formal system verification testing together with the end usersSupport other projects during research phase of product development. What you need: Required Qualifications: Proficient in SDLC, Test Methodologies, Bug Lifecycle, Test Case development, Risk Assessment3-7 years of work experience with educational qualification: B.E/B. Tech in Computer Science, MCA or any equivalent qualification.Prior experience in development and execution of application system testing in a product development environment.Prior experience in Automation testing using Python.Working experience in teams following Agile methodology.Prior experience in non-functional testing which includes accuracy, reliability, performance Preferred Qualifications: Excellent at designing and review of test case, test plan, test reports.Analytical, restorative, and strong communication skills. 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.

What you will do: Complaint Handling – Review of Complaints as received from various sources (sales Reps / Health Care professionals etc. as per approved SOP and IMDR 2017).Reporting of complaints in Stryker standard System followed by end-to-end closure. Coordinating with Division and Service for product returns/ investigation and closure of received complaints. Coordinating with service for TSR for submission into the Stryker Complaint reporting system for raised complaints.Preparation and maintenance of Complaint / SAE trackers. Evaluation of complaints for reporting to CDSCO / MvPIResponding to Hold, Recalls initiated by Division and timely evaluation and reporting to local authorities in India. Preparation of MDSAE form for IPC and CDSCO. Maintaining Label Master for Imported product & periodic review and updates of applicable SOP and Work instructions & responding to internal / external auditsISO 13485 understanding & warehouse supportPreparing and updating checklist of documentation required for New Product Registration/ License Retention / Market Standing Certificates/ Non-Conviction certificates / Test Licenses etc.Reviewing of technical Dossiers as per IMDR 2017. Preparing and drafting the DMF and PMF for registrations of all classes as per IMDR 2017. Preparing checklist of PAC as per IMDR 2017Working with CDSCO authorities to ensure zero defect New Product filings & timely submissions to CDSCO basis New Product launch timelines and securing their approvals to enable product launches in India & renewal of product licenses as and when needed Follow up with CDSCO on current and new submissions & responding to change notification and impact analysis for India. Good documentation practice for submission & labelling requirement for Medical Devices under various Act. Maintaining product approval data base & working knowledge of SUGAM and other Govt portals for files updates.Tender and Institutional support to sales team for documentation: Preparing and sharing the documents as per the requirements of Tenders. BIS Regulations & awareness of EUMDR Regulations, knowledge of recent amendments in IMDR 2017Preparing and maintaining a Monthly dashboard for International and Local communication. Preparing power point updates for Monthly Meetings & to prepare QMS procedure through the change control process. Execute the change control process in the Windchill system (one PLM) & CIDT – To Review received changes in CIDT and execute the change process. What you need: BS in Engineering, Science, or related degree; or MS in Regulatory Science6 to 10 yrs experience in to RA & quality 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.

What will you do: Plan machining projects by studying work orders, engineering plans, materials, specifications, orthographic drawings/CAD models, reference planes, locations of surfaces, and quality parameters; interpreting geometric dimensions and tolerances (GD&T). Build and develop mechanical prototype, machining fixtures.Planning, organizing, reviewing & execute in-house requests of machining prototypes.Prepare multi axis CAM programs, verify, simulate for safety & efficiency.Technical discussion with divisional/internal stakeholders and finalize on quality and timeline commitment of prototypes.Communicate & Coordinate within the team for delivery on time.Co-ordinate with machine manufacturers, tooling suppliers & software developers to drive application support, process optimization & enhance efficiency.Collaborate with the internal maintenance team & external supplier to ensure preventive & breakdown maintenance are performed on time.Initiate Non-Conformances if any prototype goes out of specification.Understand technical requirements from requestor & communicate within team for prototype development.Perform inspection of all prototypes developed in-house before delivery to requestors.Continuous follow up to ensure on time delivery of prototypes.Co-ordinate with different stakeholders for smooth execution of prototype development.Generate report on different KPIs related to in-house machining activity.Initiate DFM discussions with project team for manufacturing feasibility. Inspect completed work for conformance to specification using tools such as calipers, height gauges, micrometers, rulers etc.Accomplishes organization goals by accepting ownership for accomplishing new and different requests, exploring opportunities to add value to job accomplishments, respecting the criticality of requirements.Communicates with supervisor to offer suggestions pertinent to equipment, process needs & improvements.Provide input on Capex, Opex & budget planning and performs other duties as directed. What you need: Basic Qualifications: Education: Degree in Mechanical engineering/Tool and Die making or equivalentExperience: 6-8 Years in a manufacturing (Aerospace/Medical/Tool room/R&D/Prototype) setupMinimum 6 years of experience with multi axis machine operation, 5 axis CAM programming & hands on operation on latest machining technologies like Turn-Mills, Wire-cut, EDM, 3Axis Mill, Turning Machines, tool setup, editing and inspection in prototype and production environments.Experience with CAD/CAM software like hyperMILL, Unigraphics – NXAble to read & interpret technical drawings with GDnT.Manufacturing Proficiency – Hands on experience to run CNC Machines like Turn-Mills, Mills, Turns, & 5 Axis Machines.Work well independently and within a team and can coordinate efforts with fellow co-workersConsiderable knowledge of the cutting tools, equipment, material, methods, and standard practices of the trade.Must be adaptable to a changing work environment and competing demandsExperience with planning, estimating and reporting.Familiarity with manufacturing excellence includes modern techniques based on lean manufacturing, 5S, waste elimination and visual communication and a demonstrated ability to address practical problems and make decisions Preferred Qualifications: Software Proficiency – Power BI, Microsoft Office.Manage, motivate and engage a team of talented resources.Excellent communication skills, both written and oralExcellent attention to detail the challenges and propose solutions.Needs a strong appreciation of the importance of completing tasks on time 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.

What You Will Do- This role will lead and evaluate risk management and usability activities and systems for Joint Replacement products currently in the field in accordance with ISO 13485, ISO 14971 and IEC 62366. And lead the Risk Management Process through risk Management Principles. This role will provide direction and partner with technical and managerial leaders on emerging issues (NC/CAPA, Regulatory Requests), Joint Replacement Lifecycle Management (Product Transfers, Supplier Initiated Change Requests), and Base Business Requests (Risk Management Periodic Review, EUMDR Compliance, Health Risk Assessments). Proficient in risk management practices and tools, having high expertise in failure modes associated with production and production related processes, (PFMEA). Responsible for establishing evaluation of process risks, risk mitigation and ensures appropriate production and process controls are identified, qualified, and implemented throughout the product manufacturing lifecycle (from incoming of materials/components, manufacturing, until product release) through robust pFMEA. Ensure all Risk Management outputs comply with ISO14971. Support Design team to complete CQA/CTQ identification and inputs to dFMEA This role will establish and influence guidance documents and internal trainings to cross functional teams on areas of experience for risk management and usability, as well as present externally in audits on our risk management files. This role will seek out and drive collaboration with cross functional partners from various groups including Product Development, Regulatory, and Clinical to solve technical problems regarding our existing orthopedic products This role will represent Design Assurance and direct risk management strategy in global initiatives to improve the cost and manufacturing on Stryker devices. This role will identify, evaluate and lead continuous improvements projects within the Design Assurance team to implement new efficiencies into daily deliverables and large-scale tasks This role will be a part of a global team that drives engineering activities in the maintenance of orthopedic products to ensure the highest level of product quality and ensure compliance to the company’s quality system and external standards. This role will be on a team whose mission is to efficiently drives rigor in Sustaining activities through creative problem solving and ensures market continuity of safe and effective products. What we need- Required: Minimum of 8 years experience in quality, engineering and/or risk management in a highly regulated industry. Bachelor's Degree in engineering Experience with ISO 13485, ISO 14971 and/or IEC 62366. Experience in quality concepts (risk management, audits, NC/CAPA, HRAs). Strong interpersonal skills, written communication, and oral communication. Preferred: Medical device industry experienceClinical knowledge of Orthopadics industry. Strong analytical skills; Effective interpersonal skills and Strong communications skills.Exposure in working with cross functional team and influencing without authority. 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.

What will you do: Design and implement automation test frameworkWriting scripts to manage real time problemsWrite functional verification scenariosExecute tests and analyze results and improve test processes.Collaborate with development teamAnalyzing Code DifferentialsTest Report AuthoringEnsure Software Quality What you need: Required Qualifications: Minimum 3-6 years of Senior Software Engineer - SDET experience along with educational qualification as B.tech/MCA or any equivalent qualification..Net Framework, OOPS concepts and C/C++, C#Agile development model and Test Automation.Experience with Jenkins & BitbucketPTC Integrity/Jama (or any other relevant test management tools) Preferred Qualifications: Knowledge on WinAppDriver, FLaUI & JIRAMedical Device Industry experience 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.

What you will do- Lead the team in the development of the project charter and project management plan. Define, direct, manage, and monitor project activities to ensure alignment with business goals. Evaluate trade-offs within the project, considering scope, schedule, cost, and risks. Meet with stakeholders to define and refine project scope and seek approval from management. Develop a detailed Work Breakdown Structure (WBS) and manage the project Gantt chart. Analyze the critical path and manage major workstreams. Collaborate with supervisors and project PMs to establish and monitor project budgets. Partner with the project team to develop Project Quality Plans using quality planning tools and techniques. Monitor and maintain quality plans to ensure compliance with industry standards. Develop and implement a Risk Management Plan, identifying, analyzing, and responding to project risks. Contribute to the development of a Procurement Management Plan and collaborate on procurement partner selection. Estimate, acquire, and assign project team resources. Define team roles, responsibilities, and deliverables. Provide feedback on team performance to functional managers. Develop and execute a Stakeholder Management Plan, ensuring stakeholder expectations are managed effectively. Implement a Communications Management Plan to keep all stakeholders informed. Minimum Qualifications: Required Bachelor’s degree (BS or equivalent) and 6+ years of work experience. Previous experience in Medical Devices. Intermediate proficiency in English. Preferred Qualifications: PMP Certification or equivalent preferred. Strong knowledge of Project Management methodologies and industry best practices. Experience with quality management systems, risk analysis, and procurement processes. Proven ability to lead cross-functional teams and manage complex 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. Show more Show less

What you will do: Review & approval co-ordination of labeling jobs. Main tools are Microsoft Teams Planner and onePLM Translation coordination of labeling and regulatory documentation, professional communication with external vendors Publication and/or uploading of approved documents on global portalsSupporting labelling system for periodic updates & reports Print current labels for Regulatory Authority registration requests & Support with printing current/updated labels during mass changes Represent Global Labeling as Local Project Coordinator on major projectsProcess and implement labeling related change requests (ECR/ECN), support with the coordination of ECR related activities. Support Labeling updates/revisions, graphic design including stakeholder management Utilize and comply with Stryker’s Quality Management System including proactively verifying if requirements are met and managing changes within the Quality System Review quality assurance documentation to support mainly product sustenance and product life cycle management. Support risk management activities for Sustenance projects - Ensure that risk measures are conducted in accordance with State-of-the-Art requirements and are implemented correctly into the labeling. Taking care of timely and quality deliverables for assigned projects.Work as point of contact for all people related aspects with the stakeholders and review meetings with the team to monitor progress of projects and provide guidance, develop contingent plans, and arrange resources as needed. What you need: Strong Work experience: 7-10 years out of which 5+ years’ experience in designing, writing, and publishing technical documentation (labelling/technical publication/collateral materials) and/or Design Quality Assurance) or new product development (medical devices) Knowledge of EU MDR changes, ISO 14971, IEC 62366, Quality Concepts (e.g. CAPA, Audits, Statistics) preferred Must possess strong project management skills as well as can manage multiple tasks simultaneously Demonstrated ability to advocate for product excellence and quality. Ability to brainstorm potential solutions and execute acc. to plan Knowledge in systems and databases, preferred onePLM (CAII ideal), sharepoints and online applications A relevant bachelor’s degree (science/engineering) Excellent verbal and written communications. Great organization, capability to follow a given plan 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. Show more Show less

What will you do: Basic knowledge and understanding of complaint handling process as required by regulatory agencies. Provide updates within Trackwise on status of product field action executions and event detail information. Monitor and facilitate product return for complaint investigation and analysis, including communicating directly with customers and sales teams. May support international and domestic complaint entry. Work with internal supporting teams on quality of data coming into post market May monitor, create, and assign regulatory communications to quality specialists for resolution. What you will need: Basic Qualifications: 2+ years relevant experience required Basic knowledge and understanding of complaint handling and product field action process as required by regulatory agencies Basic knowledge on Trackwise Basic understanding of how to comply with constantly changing regulatory procedures preferred Preferred Qualifications Must possess strong interpersonal skills including written and oral communication. Must be able to bring tasks through to completion with minimal supervision. Must have the ability to prioritize work and keep detailed and confidential records. 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. Show more Show less

What Will You Do: Develop and maintain integrated software verification activities within a software development cycle, with limited supervision and author test protocols to cover software requirements. Perform software verification executions, debug, and resolution of issues. Produce complete, concise, clear and technically correct work outputs. Create and track software defect records in the defect tracking database. Report passed and failed requirements to the test team lead or program management. Apply the following software languages: C/C++, Python, Squish to the software test development with limited supervision and utilize the requirements management systems (JAMA) independently. Drive initiatives to improve product testing and design assurance processes, including suggesting technical enhancements and evolving best practices and tools. Support test reviews of various deliverables and be independently able to handle end to end feature testing and overall system testing. What Will You Need: Basic Qualifications: Bachelor’s degree in software, computer science or related discipline. 4-8 years of product testing in a product development environment or equivalent environment Basic knowhow of technology stack: C, C++, Linux, Application testing Preferred Qualifications: ISTQB and standard Agile certifications like CSM, SaFe Agile. Advanced knowledge of software verification activities integrated within a software development cycle. Experience with designing and implementing automated testing scripts. Advanced knowledge of software configuration/version control and bug tracking tools. Experience with software test equipment and test methodologies. Experience in a medical device or regulated product development environment, Software Development Life Cycle processes and in using Application Lifecycle Management /Traceability tools. Experience with regulatory and compliance standards applied to the SDLC (Software Development Life Cycle).Knowledge of automation/programming frameworks like Python, Squish etc 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. Show more Show less

Key Responsibilities: Develop, implement, and maintain the QMS in alignment with ISO 13485:2016 standards. Create, review, and update QMS documentation, including quality policies, procedures, and work instructions. Support during External (Notified Body for ISO 13485:2016) and Corporate Audits and Provide real-time support to the auditors by delivering requested documents, records, and evidence. Maintain and update the Document Control System (Windchill) for controlled documents, including SOPs, work instructions, forms, and records. Ensure document revisions, approvals, and distribution align with company policies and regulatory requirements (ISO 13485, FDA, EUMDR, etc.). Coordinate with cross-functional teams to review and approve documentation. Maintain the periodic review the documents. Maintain and update the Learning Management System (SLMS) with training records. Track training completion rates and generate reports for management and audit purposes. Communicate training requirements to employees and provide reminders for upcoming deadlines. Assist in evaluating training effectiveness through feedback collection and performance metrics. Support internal and external audits by providing training records and evidence of compliance. Qualifications & experience: Education and Experience: BSC Biotechnology, B-Pharm / M-Pharm or related field from premier institutes 2-3 years of experience in Medical Device domain At least 1+ years of experience in training and Document controller. Skills: Strong analytical and problem-solving skills. Excellent written and verbal communication skills. Proficiency in QMS software and tools. Nice to Have : ISO 13485:2016 certification Soft Skills Excellent communication & interpersonal skills. High analytical skills. Able to run communicate effectively with senior leadership. Excellent problem-solving skills. Proactive to support both internal and external customers. 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. Show more Show less

What you will do: Technical Responsibilities: Conduct or design prototyping and bench testing Conduct problem solving, identify potential solutions, and evaluate them against component and sub-system requirements Conduct research and studies to support product design Translate design inputs to engineering specifications and produce component and sub-system level designs Code development time/resource estimation to support projects Design new components applying various design concepts Generate and review the necessary documents with project teams (requirements, design, architecture, bugs, test) Business Responsibilities: Demonstrate advanced understanding of customer needs and design inputs Demonstrate proficiency with product’s intended use and clinical procedures Learn how the financial models are constructed Med Device Compliance: Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements Independently create or refine engineering documentation, such as the Design History file Follow R&D procedure like design controls and risk management, per the Quality Management System General Responsibilities: Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success as a key member of the team, collaborating with others and solidifying relationships Quickly process and assimilate procedures, policies, processes, systems, and technology required Work on complex problems, applying advanced experience and learnings Demonstrate ownership and prioritize work with minimal supervision Build relationships and influence among peers Lead code reviews for components in systems applying design principals, coding standards and best practices Develop and design software components per requirements and architecture defined What you need: Minimum Qualifications (Required): Bachelor's degree in Software Engineering/ Computer Science or related discipline & 2+ years of work experience Preferred Qualifications (Strongly desired): Technical Skills: Exposure to programming skills. Design new components applying various concepts design concepts and patterns Design and Development Skills: Experience with integrated development environments (IDE) for projects Experience with software tools for static/dynamic analysis, memory management, code coverage and techniques for analyzing software Integration and deployment processes experience Software Process Skills: Experience in creating estimates for code implementation time/resource for assigned tasks Experience in Software Development Life Cycle processes Experience using Application Lifecycle Management /Traceability tools Experience with regulatory and compliance standards applied to the SDLC (Software Development Life Cycle) 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. Show more Show less

What you will do: Design and develop high-performance mobile applications for iOS and Android (native or cross-platform). Integrate applications with Azure services such as App Services, Functions, Storage, and AAD. Conduct prototyping, bench testing, and technical feasibility assessments. Solve complex problems, evaluate solutions, and translate design inputs into engineering specifications. Estimate development time and resources for assigned components. Design new components using modern design principles and patterns. Participate in code reviews, architecture discussions, and technical documentation creation. What you will need: Basic Qualification: Bachelor’s degree in Software Engineering, Computer Science, or a related field. 4+ years of professional experience in mobile application development. Extensive experience with Swift (iOS) Experience with RESTful APIs and secure data handling. and skilled with modern IDEs (Xcode, Android Studio, Visual Studio). Familiar with tools for code analysis, memory management, and debugging. Knowledge of design patterns and mobile architecture (e.g., MVVM, Clean Architecture). Preferred Qualifications: Experience with SDLC in a regulated environment. Cross-platform tools like Flutter or React Native. Strong knowledge of Azure cloud services, including App Services, Azure Functions, Cosmos DB, and Azure AD B2C. Familiar with CI/CD pipelines and tools (Azure DevOps, GitHub Actions). Proficiency with traceability and application lifecycle management tools. 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. Show more Show less

What you will do: Technical Responsibilities: Design, develop, test, and maintain scalable web applications using the Microsoft .NET stack (C#, ASP.NET Core, MVC). Build intuitive and responsive front-end interfaces using HTML5, CSS3, JavaScript, and frameworks such as Angular, React. Develop and consume RESTful APIs and work with databases (SQL Server, Entity Framework, LINQ). Collaborate with cross-functional teams including product managers, UI/UX designers, QA engineers, and other developers. Participate in code reviews, architectural discussions, and Agile/Scrum ceremonies. Write clean, maintainable, and efficient code following best practices and coding standards. Troubleshoot, debug, and optimize application performance and scalability. Ensure the security, performance, and reliability of applications. General Responsibilities: Work cooperatively with R&D, Quality, Regulatory, Clinical, Marketing and Project Management to ensure project success as a key member of the team, collaborating with others and solidifying relationships Quickly process and assimilate procedures, policies, processes, systems, and technology required Work on complex problems, applying advanced experience and learnings Demonstrate ownership and prioritize work with minimal supervision Build relationships and influence among peers Lead code reviews for components in systems applying design principals, coding standards and best practices Develop and design software components per requirements and architecture defined What You Need Minimum Qualifications (Required): Bachelor's degree in Software Engineering/ Computer Science or related discipline & 3+ years of work experience Technical Skills: 3+ years of experience as a Full Stack Developer with a focus on .NET technologies. Proficiency in C#, ASP.NET Core, .NET Framework, and MVC. Strong understanding of front-end frameworks/libraries such as Angular, React. Experience with JavaScript, jQuery, Bootstrap, and modern CSS. Hands-on experience with SQL Server and writing complex queries, stored procedures, and database design. Familiarity with version control systems (e.g., Git) and CI/CD pipelines. Knowledge of Azure or AWS cloud services is a plus. Preferred Skills: Experience with WPF (Windows Presentation Foundation) for building rich desktop applications Knowledge of InstallShield for creating Windows installers and deployment packages Familiarity with Azure DevOps for CI/CD, project tracking, and version control integration Understanding of Jenkins Pipelines for automating build and deployment workflows 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. Show more Show less

What you will do: Ensuring compliance to Supplier Control activities identified by organization. Hands on experience of PPAP associated with New Product Launches and Management of Production cycles there after (Manufacturing Transfers). Participate in cross- functional teams 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) in identifying, prioritizing, communicating, and resolving quality issues - NC & CAPA. Conduct Supplier Audits (Product, Process & System) and Facilitate root cause analysis and corrective actions of supplier quality issues. Evaluating Quality data to identify process improvement opportunities within the supply chain. Coordinate Change Management & Control with Suppliers and implement changes at Supplier. 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) Review development protocols including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Special Process Validations, and Test Method Validations. What you will need: Required Qualification: B. Tech (Electronics/Electrical/Mechanical) with 2+ years of experience in Quality / Engineering / Manufacturing environment, preferably from medical industry. Proficient in advanced power BI applications. ISO 9001/13485 certification. Preferred Qualification: Working knowledge of basic and advanced Quality tools such as Six Sigma, SPC, FMEA, Control Plans, Root Cause Analysis, Poke Yoke, Kaizen, Lean Manufacturing etc. Strong communication skills. Must demonstrate the ability to communicate up/down and across different levels of the organization. Structurally collects facts to base his/her opinions on and ensures data integrity and traceability of data is flawless 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. Show more Show less

What you will do: Complaint handling and Product investigations of medical devices Perform Visual, functional, dimensional, functional inspection & RCA of field returned products. Maintain and ensure complaint files are complete and accurately reflect corresponding complaint activities. Risk management –Risk assessment Review of Process flow, DHR, Inspection plans, Measurement techniques, GRR’s etc. Review and analyze Literatures such as Clinical reports, PMCF reports, National register etc. to identify Complaints Create PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis. Other tasks as assigned by manager. What you need: Required skills: B. Tech / M.Tech Mechanical, Biotechnology with 2-5 years of work experience Hands on experience of Complaint handling and product investigations process.Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability. Hands on experience of Risk Management process as per ISO 14971 Sound knowledge on complaint handling process of medical devices will be an added advantage Applied understanding of GDP, ISO 9001 & ISO 13485 (Good to have).Good understanding of FDA 21CFR Part 822 / 820 (Good to have) Preferred skilla: Demonstrated ability to work effectively with various work groups to assure conformance to regulatory requirements, internal processes, and policies. Demonstrated ability to self-motivate, ability to prioritize tasks in a deadline-driven environment. Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams. 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. Show more Show less

What you will do Complaint handling and Product investigations of medical devices Perform Visual, functional, dimensional, functional inspection & RCA of field returned products. Maintain and ensure complaint files are complete and accurately reflect corresponding complaint activities. Risk management –Risk assessment Review of Process flow, DHR, Inspection plans, Measurement techniques, GRR’s etc. Review and analyze Literatures such as Clinical reports, PMCF reports, National register etc. to identify Complaints Create PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis. Other tasks as assigned by manager. What you need: Required skills: B. Tech / M.Tech Mechanical, Biotechnology with 2-5 years of work experience. Hands on experience of PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis. Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability. Hands on experience of Risk Management process as per ISO 14971 Demonstrated ability to work effectively with various work groups to assure conformance to regulatory requirements, internal processes, and policies. Demonstrated ability to self-motivate, ability to prioritize tasks in a deadline-driven environment. Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams. Preferred Skills: Sound knowledge on complaint handling process of medical devices will be an added advantage Applied understanding of GDP, ISO 9001 & ISO 13485 (Good to have). Good understanding of FDA 21CFR Part 822 / 820 (Good to have) 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. Show more Show less

What You Will Do This role is responsible for generating accurate statistical demand forecasts for the region using Demantra. It involves analyzing large datasets, applying statistical models, and identifying trends to drive forecast accuracy. The individual will collaborate with local market experts and global teams to optimize system usage, adopt best practices, and enhance forecast quality. Strong analytical and influencing skills are essential to align regional practices with global standards and support continuous improvement. Develop and maintain statistical forecasts by leveraging system capabilities, historical data, and advanced analytics to deliver high-accuracy projections. Partner with in-country demand planning experts to refine forecasts for key brands and SKUs, aligning with local market intelligence and business priorities. Collaborate closely as part of Demand Management Center of Excellence (CoE) and the Central Forecasting Team to optimize system usage, adopt best practices, and ensure adherence to governance and training standards. Contribute to global initiatives and lead cross-functional projects as needed. Apply strong influencing and communication skills to align regional practices with global standards, promote adoption of industry best practices, and support continuous improvement initiatives Analyze regional forecast trends and performance metrics (KPIs) to identify gaps, insights, risks, and opportunities that enhance forecast accuracy and effectiveness. Apply strong influencing and communication skills to align regional practices with global standards, promote adoption of industry best practices, and support continuous improvement initiatives. Partner with IT and Analytics teams to co-develop the technology roadmap for demand planning. Drive innovation by utilizing advanced tools such as AI/ML and automation in forecasting. Support scenario planning, exception management, and cross-functional projects. Work with global team to do process mapping and suggest and recommend improvements for S&OP process. What You Need Basic Qualification: A minimum of a Bachelor's degree. Analytics / Data science certifications preferred Fluency in English. Fluency in a second language at international divisions is a plus. Excellent, demonstrated quantitative, analytical and organizational skills Working knowledge of applying statistical principles to improve results Preferred Qualification: Minimum of 8 years working experience in statistical forecasting methods, using Demantra, SAP IBP or proprietary tools. (especially Demantra, DM & AFDM modules) Hands on forecasting and analytics experience with generating forecast, and how to tune and adjust models for better outcomes Strong analytical skills and attention to detail Exhibits a structured problem-solving mindset Experience working across teams in a matrix organization a plus Business experience in product industry, and working with large and diverse product portfolio a plus Ability to work under pressure and work with global stakeholders (as needed). S&OP / Integrated Business Planning knowledge is a plus Experience with SQL a plus 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. Show more Show less

What you will do: Lead the effort to perform root cause analyses, resolve and implement product fixes, modifications, and design enhancements. Drive design optimization at the intersection of material, process, manufacturing and clinical considerations. Provide engineering support for component obsolescence issues and product compliance to standards. Drive Change management and lead product testing as required. Support/Lead the transfer of new products from engineering to manufacturing Conduct or design advanced prototyping and testing Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations Lead creation and refinement of engineering documentation, such as the Design History file, BOM, drawings, and procedures. What you will need- Required- Minimum Qualifications (Required): Bachelor of Science in Engineering, Mechanical Engineering or BioMedical & 7.5+ years of work experience Good understanding of medical device product development, risk management methodologies, dfmea, DIOVV etc. Strong technical ability in creating engineering drawings, models, sampling plans, Design Verification Plan and Report. Preferred Qualifications (Strongly desired): Adept at applying knowledge of materials, statistics and manufacturing processes to product design Ability to communicate moderate complexity plans and technical information to team members Project management and strong organizational skills 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. Show more Show less

What Will You Do As part of product transfers of a product line that is being relocated from one site to another, you will actively shape the process development and ensuring that all activities are completed and documented in accordance with the Stryker procedures. In addition to coordinating internal and external partners, you are responsible for solving technical challenges and implementing efficient manufacturing and testing strategies in a highly technical environment. In your role, you will make a significant contribution to the realization of short transfer times, considering innovative problem-solving methods, continuous development and optimization of our manufacturing processes. As a process engineer, you work closely with cross functional teams and international project teams and process experts. Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers. Complete capability and MSA studies for in process inspection and generate subsequent Inspection documentation. What Will You Need Basic Qualification: Based on a successfully completed engineering degree (automation technology, process engineering, electrical engineering, mechanical engineering, medical technology, industrial engineering, biotechnology or similar), you ideally have 7 or more years of professional experience in the field of process development and/or process optimization. While working with a wide range of interfaces, your good communication skills, your open and positive nature as well as your committed and independent way of working. The individual should enjoy working in a fast paced, dynamic and results orientated team environment Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Excellent analytical skills, ability to plan, organize and implement concurrent tasks. Preferred Qualification: Good knowledge of manufacturing processes, materials, product and process design. Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing. Experience in an FDA regulated or regulated industry beneficial. Individual is willing to travel occasionally for business purposes. 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. Show more Show less