Associate I Quality Assurance Job At Baxter Ahmedabad
Baxter is hiring an Associate I, Quality Assurance in Ahmedabad, Gujarat, offering an excellent opportunity for pharma professionals to work in cGMP compliance, document control, batch records, and quality systems. This Quality Assurance Job role is ideal for candidates with 3–7 years of QA experience who want to contribute directly to patient safety and product quality. Graduates seeking B Pharma jobs or Pharma Jobs can apply now.
- Job Title: Associate I, Quality Assurance
- Location: Ahmedabad, Gujarat, India
About the Company
Baxter is a global healthcare leader dedicated to improving patient outcomes through innovative medical products and therapies. Founded in 1931, Baxter’s mission to Save and Sustain Lives continues to guide its commitment to quality, safety, and operational excellence. Quality at Baxter spans the entire product lifecycle, offering employees meaningful work and long-term career growth. This Quality Assurance Job role plays a significant role in the company.
Key Responsibilities
- Manage Document Control activities under guidance of QA Head or Supervisor
- Ensure compliance with current Good Manufacturing Practices (cGMP)
- Review and verify GDP compliance and address documentation gaps
- Issue, close, archive, retrieve, and manage Logbooks, BMRs, BPRs, and standard formats
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) for new and commercial products
- Prepare and review BMRs/BPRs using Technical Packages (TP) and site processing parameters
- Maintain Bill of Materials (BOM) and create HALB codes in JDE
- Review and update SOPs for QA and cross-functional departments
- Prepare Annual Product Review (APR) reports for regulatory dossier updates
- Handle Change Control Management (CCM), Document Change Requests (DCR), NCR, CAPA, and investigations
- Support stability documentation and generate stability intimation slips in ELN
- Resolve batch record queries and support cross-functional teams
Educational Requirements
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B. Pharm
Experience Required
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3–7 years of experience in Quality Assurance / Document Control within a pharmaceutical organization
Skills Required
- cGMP and GDP compliance
- Document Control and QA systems
- BMR / BPR preparation and review
- SOP writing and revision
- Change control, CAPA, NCR handling
- Regulatory documentation knowledge
- Strong attention to detail and data integrity
- Cross-functional communication skills
Why This Job Role?
- Work with a globally respected healthcare company
- Direct impact on patient safety and product quality
- Exposure to end-to-end QA systems and regulatory compliance
- Strong learning, career growth, and internal mobility opportunities
- Purpose-driven role aligned with Baxter’s life-saving mission
- Graduates seeking B Pharma jobs or Pharma Jobs can apply now.
