Global healthcare company Baxter is currently hiring for the position of Associate I – Quality Assurance in Ahmedabad, Gujarat. This opportunity is ideal for professionals interested in pharmaceutical quality assurance, batch disposition, deviation investigation, and GMP compliance.
Baxter is recognized worldwide for its mission to Save and Sustain Lives, making it a leading employer in the pharmaceutical and medical device sector. The Associate I Quality Assurance role at Baxter Ahmedabad focuses on ensuring compliance with quality standards, reviewing manufacturing documentation, and supporting regulatory and quality operations.
Professionals with experience in pharma QA operations, batch release review, deviation management, and regulatory compliance are encouraged to apply.
Job Details
| Field | Information |
|---|---|
| Position | Associate I – Quality Assurance |
| Company | Baxter |
| Location | Ahmedabad, Gujarat, India |
| Job Type | Full Time |
| Application Deadline | 27 March 2026 |
| Department | Quality Assurance |
| Industry | Pharmaceutical / Healthcare |
Key Responsibilities
The Associate I Quality Assurance professional at Baxter will be responsible for ensuring pharmaceutical manufacturing processes meet regulatory and internal quality standards.
Key duties include:
- Perform batch disposition after reviewing batch manufacturing, packing, and testing records in compliance with SOPs and specifications.
- Ensure investigations related to batches are closed before batch release.
- Conduct impact assessment for change control proposals affecting batch release functions.
- Investigate deviations, discrepancies, and non-conformities in manufacturing or documentation.
- Place affected batches on hold or quarantine until final disposition.
- Investigate out-of-specification (OOS) events and market complaints to determine root cause and patient safety impact.
- Identify batches with quality non-conformance and ensure proper rejection and destruction procedures.
- Prepare Certificate of Conformity (CoC) and Certificate of Manufacturing (CoM) documentation.
- Verify serialization data and EMV compliance before CoC preparation.
- Manage on-status batch shipment processes and QA documentation coordination with warehouse teams.
- Maintain daily batch release and rejection trackers.
- Support Regulatory Affairs and Product Assurance teams for quality-related queries.
- Assist in responding to regulatory authority and government queries regarding released products.
- Support continuous GMP compliance and quality improvement initiatives at the manufacturing site.
Required Qualifications
Candidates applying for the Baxter Associate I Quality Assurance job should possess:
- B.Pharm / M.Pharm / MSc (Life Sciences / Pharmaceutical Sciences) or related qualification
- Knowledge of Good Manufacturing Practices (GMP)
- Understanding of batch manufacturing records (BMR), deviation management, and change control
- Familiarity with pharmaceutical quality assurance systems
- Strong documentation, investigation, and compliance skills
Preferred skills:
- Experience in pharma manufacturing QA
- Knowledge of OOS investigations and CAPA
- Exposure to regulatory compliance and audit readiness
Salary and Benefits
Estimated salary range based on industry benchmarks:
- ₹4,50,000 – ₹7,50,000 per year (INR)
Additional benefits may include:
- Health and wellness programs
- Global career growth opportunities
- Learning and development programs
- Inclusive workplace culture
- Exposure to global quality and regulatory systems
Why Join Baxter?
Baxter is a global healthcare leader committed to improving patient outcomes. Employees benefit from:
- Mission-driven work focused on saving and sustaining lives
- Opportunities to work in advanced pharmaceutical manufacturing environments
- Global collaboration across regulatory, quality, and clinical teams
- Strong culture of innovation, accountability, and professional growth
How to Apply
