Job Description

Vantive: A New Company Built On Our LegacyBaxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.At Vantive, you will become part of a community of people who are focused, courageous and don\xe2\x80\x99t settle for the mediocre. Each of us are driven to help improve patients\xe2\x80\x99 lives worldwide. Join us as we revolutionize kidney care and other vital organ support.*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.About BaxterBaxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis;sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacyautomation, software and services. The company\xe2\x80\x99s global footprint and the critical nature of its products and servicesplay a key role in expanding access to healthcare in emerging and developed countries. Baxter\xe2\x80\x99s employees worldwideare building upon the company\xe2\x80\x99s rich heritage of medical breakthroughs to advance the next generation of healthcareinnovations that enable patient care.Job Summary

• Job Title \xe2\x80\x93 Senior Engineer, Sterility Assurance, Solutions

• Location \xe2\x80\x93 Whitefield, Bangalore

This position is primarily responsible for the planning, designing, execution, documentation, data analysis and final report generation for sterilization cycle development, process qualification and Sterility Assurance studies for Solutions, drugs and devices. The candidate should have a strong background of sterilization Validation and should have a strong understanding of the scientific aspects related to sterilization and Sterility Assurance.The Sterility Assurance Engineer will be required to have the knowledge required to provide support in the following.Good understanding of the Science & Sterilization principles, guidance, regulations around sterilization validation & related to Sterility Assurance for Solutions. Design, development &Technical Understanding of Validation & Sterilization Engineering principles for Solutions and or devices.

• Planning, execution, and documentation of sterilization cycle development for Moist Heat Sterilization, (Knowledge of Ethylene Oxide sterilization, Radiation sterilization will be an additional skill)
• Good understanding of Life Cycle of sterilization development, Assessment of result & to verify if anything goes wrong in the process.

Solid Leadership skills, team orientation and understanding of organizational cultural attributes.Candidate working with a Device Development Company- Research and Development, Quality Assurance, Validation, Sterilization, Sterility Assurance, Regulatory but should have a good knowledge of Regulations and GMP working environment. Exposure to product life cycle, Research and Development and product delivery is strongly desirable.Essential Duties and Responsibilities

• Contribute to technical feasibility analysis of complex research and design concepts including microbiology inputs for sterility assurance and related controls for the Solutions and devices/disposables.
• Play a lead role in the evaluation, selection and adaptation of various techniques, which accomplish business objectives such as quality, cost optimization and cycle-time.
• Design and perform Sterility Assurance Assessments and Sterilization qualification & validation studies in support of medical device, Solutions & pharmaceutical projects.
• Perform standard sterilization engineering assignments for application, validity and conformance to specifications.
• Utilize analytical process tools to solve complex process problems (e.g., FMEA, Risk Analysis, Process Modeling, Design of Experiments). Lead small project teams as needed to accomplish project objectives.
• Study and recommend techniques to improve existing products/processes and process controls.
• Provide sterilization support for Renal R&D projects and technical trouble shooting & to evaluate results relative to product requirements, definitions and/or program goals
• Analysis and evaluation of sterilization studies data and assist in the preparation of documentation using Good Documentation Practices (GDP).
• Employ appropriate techniques and methods to successfully conduct specific assignments within negotiated deadlines after receiving general instruction.
• Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks.
• Devise new approaches to complex problems through adaptations and modifications by use of standard technical principles.
• Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to R&D (product development, design, and safety) to ensure compliance in all research, data collection and reporting activities.
• Develop reports and presentations on technical plans and results.
• Display a solid understanding of theories/practices utilized by other disciplines outside primary area of expertise.
• Ability to convince management on courses of action with minimal assistance using both written and verbal methods.
• Knowledge around microbiological aspects of biological indicators, Adventitious Agents and related microbiological concepts.

Qualifications

• Master\xe2\x80\x99s degree in a scientific discipline (Engineering &Technology) with minimum 6 years or BS with minimum 8 years\xe2\x80\x99 experience in sterilization validation or equivalent.
• Prefer experience with Sterilization Validation, Device/Product Development Lifecycle, Global sterilization regulations & TQM methods (e.g. "six sigma")
• Display a solid technical understanding of Sterilization Engineering principles and qualification practices for Solution Sterilization & application of these principles on individual/small projects.
• The position requires technical skills for Solution sterilization using Moist heat (Steam), assessing critical changes & impact assessments, writing study rationale documents.
• Technical writing skills, remote support for projects, strong interpersonal skills and with a quick adaptive mindset for the new technologies.

Skills

• Excellent English verbal and written communication skills, skilled to coordinate with global stake holders and support across the different time zones.
• Proficient with Sterilization validation principles and related testing for Biological indicators etc.
• Hands on experience cycle design and development and performing the sterilization studies for solutions with use of biological indicators.
• Highly adept at grasping and solving complex problems using root-cause analysis techniques.
• Ability to objectively identify technical solutions and make sound decisions
• Project management experience for Quality & value improvement projects
• Self-driven, resourceful, and able to work on multiple projects and priorities.
• Strong organization, attention to detail, and documentation skills.
• Strong acquaintance with technology, QMS tools and collaboration tools over the web: e.g. Trackwise, Document tools, WebEx, Teams, Microsoft Office products, etc.

A Career That MattersBaxter\xe2\x80\x99s employees are united in a mission to save and sustain lives. We are passionate about applying scientificinnovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies andtechnologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuingcreative collaborations that bring our mission to life for patients every day.Equal Employment OpportunityBaxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion,gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any otherlegally protected characteristic.Reasonable AccommodationsBaxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the here and let us know the nature of your request along with your contact information.Recruitment Fraud NoticeBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our .

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