Analyst IT

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Title: Analyst, IT – Validation Lead

Location: Bangalore

Your Role

This position is accountable for performing activities in support of the validation and compliance of a computerized system to ensure the system meets its intended use. This position will work with IT team(s) to ensure a computerized system is compliant with applicable regulations (21 CFR Part 11, GxP Regulations) and Baxter Quality Management System requirements.

Support the Validation activities during the deployment of any new GxP Application.

What you’ll be doing

• Review project teams' work to ensure quality (design walk-through, code review, test results, etc.) and alignment to the processes, standards, and regulatory requirements.
• Responsible for the conduct of Verification and Validation activities as per requirements defined in Baxter Design Control Method and regulatory requirements.
• Responsible for assuring the new Computerized System meets the requirements of the systems users & Regulatory requirements.
• Creating, managing, and /or maintaining the documents required by Baxter quality systems procedures for the development and validation of the Computerized System.
• Responsible for oversight of protocol execution.
• Shall control the Validation Package and shall ensure that all documents contained in the Validation Package are maintained per document retention policies/procedures.
• Coordinate risk management of new or changed computerized Systems.
• Ensure design review and application acceptance including completeness of Trace Matrix (link among user requirements,  functional requirements, design requirements and test plan)
• Communicate and control the adherence to validation standards by the team.
• Provide support to the functional team/users for the development of validation deliverables (functional specification, technical specification, system & user procedures, etc).
• Support the processes to maintain in a controlled state of validation during the entire life cycle of Computerized Systems.

What you’ll bring

• Bachelor’s degree in science, engineering, or technology and meaningful work experience required.
• 3+ years of Quality or IT system development experience is required.
• Good knowledge of GxP regulations (e.g. 21 CFR Part 11, GAMP 5, MHRA etc.), Standards, and Industry Best Practices.
• Good communication skills.
• Strong knowledge of software development/implementation processes.
• Knowledge and experience in the following areas:
  • Documentation Management using document management tool.
  • Test Management tool Micro Focus ALM

EEO (Equal Employment Opportunity)

Baxter 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, protected veteran status, disability/handicap status or any other legally protected characteristic.

Equal Employment Opportunity

Baxter 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, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter 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 link here and let us know the nature of your request along with your contact information.

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