Jobs at Baxter International Inc.

Supports supply chain analytics users through troubleshooting, training, documentation, data validation, and report deployment. Maintains data quality for sprint reporting, leads weekly development sprint calls, removes project roadblocks, escalates data issues, and provides ad hoc analytics. The role partners with supply chain planning teams to identify reporting gaps and improve analytics tools and processes.

Prepare, pick, dispense, check, store, and dispatch medicines for homecare patients. Maintain accurate system records, follow GDP, GWP, SOPs, batch control, and FEFO principles, complete quality and compliance checks, manage returns and disposal, document incidents, and escalate discrepancies under the guidance of the Responsible Pharmacist. The role involves shift work, frequent manual handling, PPE use, and adherence to pharmacy and warehouse procedures.

Coordinate FP&A activities including cash flow projections, budgets, forecasts, strategic plans, and monthly reporting. Load forecast adjustments, analyze budget-to-actual variances, identify business and operational risks, and advise Finance leadership. Collaborate with divisional finance leaders, the Global Delivery Center, and cross-functional teams while maintaining reporting quality, controls, process documentation, and management reporting packages.

Leads electrical engineering for medical device sustenance, new product development, and product lifecycle management. Designs analog and digital circuits, power systems, and embedded controls; defines architectures, requirements, verification, validation, and test methods. Oversees EMI/EMC compliance, manufacturing transition, troubleshooting, quality, regulatory, and design controls. Coordinates engineers and technicians while collaborating with global cross-functional teams to deliver safe, compliant products and technical strategies.

Provides Tier 1 HR support through chat, email, and ticketing systems; responds to employee questions, processes Workday transactions, maintains accurate HRMS data, supports onboarding and offboarding, documents cases, meets SLAs, and escalates complex issues. The role also supports audits, compliance, employee documentation, and HR process improvements while working rotational shifts across regional operations.

Supports quality and operational improvement activities, including Kaizen events, corrective actions, process improvement projects, action planning, and Quality Management System effectiveness. Collaborates with cross-functional teams, collects and analyzes data, prepares reports, and helps implement improvements under supervision. Requires strong organization, analytical thinking, communication, teamwork, multitasking, and proficiency with Microsoft Office tools.

Provide senior-level individual contributor oversight of QMS processes (change control, CAPA, complaints, nonconformance), lead complex quality investigations, prepare management-review materials and metrics, support audits/inspections, maintain inspection-ready eQMS records, and coach cross-functional teams to drive compliant, timely resolution and continuous improvement.

Leads margin improvement, medical device manufacturing, and new product projects. Identifies cost-saving opportunities, evaluates feasibility and savings, coordinates multidisciplinary teams, manages schedules and budgets, and leads Kaizen, VAVE, and workshop events. Develops and executes process validations, including IQ, SV, DOE, OQ, PQ, and TMV, while ensuring compliance with FDA quality system requirements, ISO standards, and GMPs. Supports process improvements, line transfers, CAPEX/OPEX planning, and team development.

Manufactures, assembles, packages, labels, and kits medical device products while following GMP, GDP, safety, and quality procedures. Operates production equipment, proofreads labels, stocks finished goods, distributes supplies, cleans production areas, and handles hazardous materials and waste. Requires attention to detail, teamwork, basic math, frequent hand coordination, and the ability to stand or sit for extended periods and lift up to 65 pounds with a team.

Lead laboratory investigations involving particle identification, failure analysis, root-cause analysis, and manufacturing process capability. Design experiments, use advanced microscopy and spectroscopy to characterize materials, evaluate data, and provide technical recommendations. Collaborate with R&D, Quality, and Manufacturing teams on product and process development, continuous improvement, and feasibility assessments. Ensure research documentation and reporting comply with quality, safety, regulatory, and GxP requirements.

Supervise manufacturing operations, production scheduling, staffing, materials, training, compliance, audits, and documentation. Lead personnel development, product release support, FDA inspection readiness, investigations, troubleshooting, equipment validation, continuous improvement, lean initiatives, and cost-saving projects. Ensure adherence to cGMP, EHS, SOP, quality, safety, and production standards while managing multiple priorities, shifts, weekends, overtime, and cleanroom activities.

Leads Baxter’s government pricing and compliance function, including AMP, BP, ASP, 340B, Non-FAMP, Medicaid rebate, VA/FSS, and state transparency submissions. Oversees pricing methodology, regulatory interpretation, outsourced calculation partners, Model N governance, reconciliation, reserves, accruals, audit readiness, and vendor performance. Advises Commercial, Finance, Legal, Marketing, and Market Access leaders on pricing and legislative impacts, including IRA-related changes. Drives process standardization, unbundling, system modernization, and special projects.

Leads end-to-end systems engineering and human factors activities for medical devices, from user and marketing requirements through product release and lifecycle management. Develops system architectures, requirements traceability, integration plans, risk assessments, usability evaluations, and verification support. Applies FDA, EU MDR, ISO, and IEC standards while resolving technical trade-offs across engineering, manufacturing, regulatory, and marketing teams. Provides technical leadership, coaches engineers, supports audits, manages budgets and timelines, and drives product quality and safety.

Drive Baxter product sales across Nashik and surrounding districts by engaging healthcare professionals, surgeons, intensive care specialists, purchasing authorities, and channel partners. Develop territories, identify customers, execute clinical selling and promotional activities, manage inventory and complaints, monitor competitors, support new product penetration, and achieve sales forecasts and KPIs. The role also involves strategic account management, market feedback, negotiations, and coordination with headquarters to support supply and cash flow.

Develop medical device systems from concept through verification and validation using systems engineering and MATLAB model-based design. Define requirements, use cases, safety and usability needs; manage risks under ISO 14971; support hardware/software integration, technical documentation, design reviews, and verification planning. Collaborate with cross-functional teams to resolve complex issues while meeting cost, quality, schedule, FDA, MDR, ISO, and IEC requirements.

Develop and maintain secure, reliable software for medical devices and connectivity products across the full software lifecycle. Responsibilities include coding, unit testing, troubleshooting, root cause analysis, technical documentation, development environment maintenance, CI/CD automation, and collaboration with Product Management, Quality, Verification, Service, and Marketing teams. The role also provides technical guidance and supports regulated healthcare software development.

Leads medical-device systems engineering and standards-compliance activities across product development and lifecycle stages. Responsibilities include system architecture, requirements decomposition, traceability, DHF maintenance, risk management, integration and validation testing, design controls, global regulatory compliance, EMC and safety testing, certification coordination, and resolution of technical issues. Collaborates with hardware, software, clinical, regulatory, manufacturing, suppliers, laboratories, and certification agencies.

Oversee Mexican and international import/export compliance, tariff classification, customs reporting, trade systems, IMMEX and VAT-IEPS certification, inventory controls, and regulatory audits. Develop policies, lead training, manage budgets, support international logistics, and drive continuous improvement. Lead and coach the Import/Export team while coordinating with manufacturing, procurement, planning, customer service, government agencies, and regulatory authorities. Ensure corrective actions, CAPA activities, Lean practices, and compliance processes meet organizational and regulatory requirements.

Leads Baxter’s Malaysia sales team to achieve revenue and gross-profit targets, develop sustainable customer business, and execute sales strategies. Responsibilities include forecasting, market analysis, territory planning, distributor coordination, key-account and opinion-leader relationships, KPI management, coaching, talent development, compliance, and collaboration with marketing, supply chain, clinical, and technical teams. The role requires travel, including visits to remote urban areas, and occasional weekend participation in business events.

Manages Baxter’s onsite third-party logistics warehouse relationship, overseeing daily operations, service levels, inventory accuracy, order and shipping escalations, KPI performance, and continuous improvement. Coordinates with planning, sales, manufacturing, suppliers, distribution, and transportation teams to optimize fulfillment, inventory costs, profitability, and customer service. Leads business reviews, resolves operational issues, and implements process improvements while ensuring safety compliance.