Job Title:
Research Associate I – SPO (Product Life-Cycle Management)
Job Requisition Number: JR-170255
Location: Ahmedabad, Gujarat, India
Company: Baxter International Inc.
About Baxter
At Baxter, our mission to Save and Sustain Lives is at the heart of everything we do. With over 85 years of pioneering medical innovation, Baxter’s products and therapies are present in almost every hospital around the world. Join us to make a global impact through meaningful work in a culture driven by purpose, innovation, and collaboration.
Position Summary
As a Research Associate I, you will be responsible for evaluating Supplier Notices of Change (SNCs) and Proposed Initiatives (PIs) related to commercialized products, and managing the entire change control process from initiation to closure. You will collaborate cross-functionally to ensure compliance, documentation, and timely implementation of product changes.
Key Responsibilities
Change Management
Act as Change Owner for product design, supplier, and registration changes.
Evaluate SNCs/PIs and manage change controls across their lifecycle: initiate, assess, review, implement, and close.
Ensure cross-functional assessments are completed in a timely and compliant manner.
Cross-functional Collaboration
Work closely with PDO, Regulatory Affairs, Project Management, Quality, CMOs, and other stakeholders to implement change plans.
Maintain strong communication and provide regular updates on project statuses.
Documentation & Compliance
Develop, maintain, and update Design & Technical documentation as per Good Documentation Practices (GDP).
Ensure compliance with Baxter’s Quality Management System (QMS) and relevant regulations (international/regional/national).
Support regulatory audits and Ministry of Health (MoH) queries by coordinating with subject matter experts.
Continuous Improvement & Innovation
Participate in or lead ideation sessions focused on product improvement and innovation.
Propose enhancements in change control processes or documentation practices.
Qualifications
Master’s Degree in Science or Pharmaceutical disciplines (mandatory)
Must be capable of engaging in technical discussions and assessments.
Experience Requirements
4–6 years of relevant experience in pharmaceutical product lifecycle management.
Strong understanding of:
Product development stages
Design control documentation
Quality Management Systems
International and regional regulatory standards
Proficiency in:
Project management
Problem-solving and analytical thinking
Oral and written communication
Task organization and prioritization
Core Competencies
Action Oriented
Collaborates Across Teams
Drives Results
Courageous & Innovative
Manages Ambiguity
Work Culture & Benefits
Support for Parents
Continuing Education & Professional Development
Paid Time Off
2 Days of Volunteering Annually
Employee Health & Well-being Programs
Equal Employment Opportunity
Baxter is an equal opportunity employer. We evaluate qualified applicants without regard to race, religion, gender, age, sexual orientation, disability, or any legally protected characteristic.
Recruitment Fraud Notice
Be cautious of recruitment fraud. Baxter does not request financial or personal information during recruitment. For more details, please review our official Recruitment Fraud Notice.
Work Location
Baxter – Ahmedabad Office
Navratna Corporate Park
Tower A, Ground Floor
Tower B, 21st and 22nd Floors
Gujarat – 380058, India
Apply Now
Click here to apply (Insert actual application link)
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