Senior Principal Mechanical Design Engineer

The Senior Principal Engineer FEA & CFD provides thought leadership in advanced simulation to support product design, development, and verification of medical devices. This role acts as a recognized technical authority for structural and fluid simulations, driving modelling strategy, solving complex engineering problems, and influencing product and technology decisions across R&D teams. The role partners closely with cross functional stakeholders to enable simulation driven development and to support regulatory compliance.

Responsibilities may include the following and other duties may be assigned:Lead advanced FEA and CFD analyses for complex medical device systems, including nonlinear structural, dynamic/impact, and advanced material modelling.Plan, execute, and review CFD simulations for internal and external flows, multiphase flows, heat transfer, fluidstructure interaction (FSI), and particle tracking.Define, communicate, and drive simulation strategies aligned with product requirements, design objectives, risk management, and verification needs.Provide actionable design guidance based on structural, thermal, and fluid behaviour insights to improve performance, reliability, and manufacturabilityModel Development, Verification and ValidationDevelop, calibrate, and maintain robust FEA/CFD models, including material models, contact definitions, and boundary conditions.Establish and maintain simulation verification and validation (V&V) frameworks and procedures to ensure model credibility and appropriate use.Correlate simulation results with bench testing, animal studies, clinical data, and relevant historical data, and document evidence in DHF and regulatory submissions.Support design verification, risk mitigation, and root cause investigations using simulation to explain failure modes and inform corrective actions.Innovation and Continuous ImprovementDrive innovation in simulation methodologies, including automation, reducedorder models, surrogate models, and digital twin approaches.Evaluate and implement emerging simulation technologies, tools, and workflows to improve efficiency, accuracy, and scalability.Develop and promote best practices, standards, and templates for FEA/CFD within the organization.Collaboration and InfluencePartner with systems engineering, design engineering, test, quality, manufacturing, and regulatory teams to integrate simulation into endtoend product development.Communicate complex simulation results and tradeoffs clearly to technical and nontechnical stakeholders, influencing design and program decisions.Represent simulation in design reviews, technical forums, and regulatory interactions as required.Coaching and Capability BuildingMentor and coach engineers in FEA/CFD methods, tools, and best practices, building a strong simulation community of practice.Lead technical reviews of simulation work products, providing guidance and feedback to elevate quality and consistency.Contribute to talent development by identifying skill gaps and supporting training plans in advanced simulation.Required Knowledge and Experience:Bachelors or Masters degree/ Phd in Mechanical Engineering or a related discipline from a recognized institution (IITs, NITs, IISc or other premier institutes preferred).Must have 20+ years of experience in simulationdriven product development, preferably in highly regulated industries.Deep, handson expertise in FEA tools such as LS Dyna, ANSYS, Abaqus and CFD tools such as Fluent, StarCCM+ (or equivalent).Proven track record of leading complex, highfidelity structural and CFD analyses and translating insights into design decisions.Demonstrated ability to independently drive multiple projects, manage priorities, and deliver highquality work in ambiguous, fastpaced environments.Strong communication and presentation skills, with experience influencing stakeholders and driving alignment across crossfunctional teams.Knowledge of simulation credibility frameworks and model risk assessment (for example ASME V&V 40), with experience contributing to regulatory submissions and technical reviews.Familiarity with ISO 13485, design controls, risk management, and product verification processes in a regulated environment.Strong understanding of materials such as metals, polymers, hyperelastic materials, and composites, and their application in simulation models.Experience across multiple medical device domains (implants, disposables, capital equipment, or other relevant product categories).Experience in design exploration and design optimization, including robust design techniques and multiobjective optimization.Exposure to or experience with digital twin technologies and integration of simulations with test/field data.Experience defining or implementing automated simulation workflows, scripting, and data management for largescale analyses.Recognized subject matter expert (SME) in simulation within the organizationProvides technical leadership across programs .