Associate I Quality Assurance Job at Baxter in Ahmedabad. Apply online for QA pharma role with batch release, GMP compliance experience.
Introduction
Quality Assurance professionals looking to work with a globally recognized healthcare company can explore this opportunity at Baxter. The organization is currently hiring for the position of Associate I – Quality Assurance at its manufacturing facility in Ahmedabad, Gujarat.
This role is ideal for candidates interested in pharmaceutical quality systems, batch disposition processes, regulatory compliance, and product release activities. The selected candidate will work closely with quality teams to ensure that manufacturing, packaging, and testing processes comply with established procedures and regulatory standards. Associate I Quality Assurance Job at Baxter
Company Overview
Baxter is a global healthcare company dedicated to improving patient outcomes through innovative medical products and therapies. Since its establishment in 1931, the company has focused on advancing healthcare solutions that help patients live healthier lives.
Operating in multiple countries worldwide, Baxter develops and manufactures products used in hospitals, clinics, and healthcare facilities. The company’s mission, “Save and Sustain Lives,” drives its commitment to delivering safe, high-quality medical products and maintaining strong regulatory compliance standards across its operations.
Baxter promotes a collaborative workplace culture where employees are encouraged to contribute ideas, maintain high ethical standards, and take ownership of their work. Associate I Quality Assurance Job at Baxter
Job Overview
| Job Details | Information |
|---|---|
| Company Name | Baxter |
| Position | Associate I – Quality Assurance |
| Department | Quality Assurance |
| Industry | Pharmaceutical / Healthcare |
| Job Location | Ahmedabad, Gujarat, India |
| Employment Type | Full-Time |
| Experience Required | As per company requirements |
| Qualification | Bachelor’s degree in relevant field |
| Application Mode | Online Application |
| Application Deadline | March 27, 2026 |
Job Location & Employment Type
The Associate I – Quality Assurance role is based at Baxter’s manufacturing facility in Ahmedabad, Gujarat.
This is a full-time position within the quality assurance department. The role involves supporting batch review processes, quality investigations, and compliance monitoring to ensure that pharmaceutical products meet regulatory standards before release. Associate I Quality Assurance Job at Baxter
Open Positions / Department Details
Position: Associate I – Quality Assurance
Department: Quality Assurance
The QA department plays a critical role in maintaining product quality, regulatory compliance, and manufacturing integrity. The selected candidate will be involved in reviewing batch documentation, supporting investigations, and ensuring compliance with Standard Operating Procedures (SOPs). Associate I Quality Assurance Job at Baxter
Key Roles & Responsibilities
Batch Review and Disposition
One of the key responsibilities of this role is reviewing batch manufacturing, packaging, and testing records. The Quality Assurance Associate ensures that all records comply with approved procedures, specifications, and documentation standards before a batch is released. Associate I Quality Assurance Job at Baxter
The role also involves verifying that investigations related to any deviations or issues are completed before final batch disposition.
Change Impact Assessment
The candidate will evaluate proposed changes that may affect batch release processes. This includes providing quality impact assessments for change control proposals and recommending appropriate actions when necessary.
Investigation of Deviations and Non-Conformities
The QA professional will identify and investigate discrepancies that occur during manufacturing or documentation processes. This includes determining root causes and ensuring corrective actions are implemented.
If necessary, affected batches may be quarantined until a final quality decision is made.
Quality Hold and Batch Investigation
In situations where quality concerns arise—such as out-of-specification results or process deviations—the candidate may place affected batches on hold.
Investigations are conducted to determine the cause of the issue and evaluate potential risks to product quality and patient safety.
Handling Rejected Batches
The role also involves identifying batches that fail to meet established quality standards. Such batches may be transferred to the rejected material area and processed for destruction according to approved procedures.
Proper documentation and traceability of packaging materials and batch records must be maintained throughout this process. Associate I Quality Assurance Job at Baxter
Certification Documentation
The candidate will assist in preparing documentation such as Certificates of Conformity (CoC) and Certificates of Manufacturing (CoM) as required by quality or business departments.
This process may also involve verifying serialization data before preparing certification documents.
Batch Shipment Control
The QA associate will support the batch shipment process by ensuring all necessary documentation is complete before a batch is released for distribution.
Coordination with warehouse teams may be required to ensure proper communication regarding batch status.
Daily Quality Reporting
The role includes maintaining a tracking system that records the status of released or rejected batches. These updates must be communicated regularly to supervisors or QA leadership.
Regulatory Communication Support
The candidate may assist regulatory affairs teams by providing quality documentation or responding to regulatory queries when required.
This may include supporting communication with regulatory authorities or external stakeholders.
Continuous Compliance Activities
The QA associate will support various compliance initiatives within the facility to ensure that manufacturing operations remain aligned with regulatory requirements and quality standards.
These activities help maintain the site’s overall compliance status and product quality. Associate I Quality Assurance Job at Baxter
Eligibility Criteria
Candidates interested in this opportunity should meet the following eligibility requirements.
Education
Applicants should possess a Bachelor’s degree in Pharmacy, Life Sciences, Chemistry, or a related discipline.
Experience
Experience requirements are not clearly specified in the job description. However, candidates with experience in pharmaceutical quality assurance, GMP compliance, or batch review processes may be preferred.
Skills Required
The ideal candidate should possess the following skills:
- Knowledge of pharmaceutical quality assurance processes
- Understanding of Good Manufacturing Practices (GMP)
- Experience with batch documentation review and release procedures
- Ability to investigate deviations and quality issues
- Strong documentation and reporting skills
- Good analytical and problem-solving abilities
- Effective communication and collaboration skills
Salary & Benefits
Salary details for this position have not been disclosed and will be as per company norms.
Employees at Baxter often benefit from a professional work environment focused on innovation, teamwork, and career development within the global healthcare industry. Associate I Quality Assurance Job at Baxter
Selection Process
The recruitment process for this role may include the following stages:
- Online Application Submission
- Resume Screening by HR Team
- Technical Interview
- HR Interview
- Final Selection
Shortlisted candidates will be contacted by the company for further evaluation. Associate I Quality Assurance Job at Baxter
How to Apply
Candidates interested in the Associate I – Quality Assurance role at Baxter can apply online through the company’s official careers portal.
Applicants should ensure that their resume clearly highlights experience in:
- Pharmaceutical quality assurance
- Batch documentation review
- GMP compliance
- Quality investigations and documentation
Providing relevant QA experience can significantly increase the chances of being shortlisted. Associate I Quality Assurance Job at Baxter
Important Dates
- Job Posted: Recently
- Application Deadline: March 27, 2026
Candidates are encouraged to apply before the deadline.
Why Apply for This Pharma Job?
Working in Quality Assurance at Baxter offers professionals the opportunity to contribute to global healthcare quality standards. QA teams play a vital role in ensuring that pharmaceutical products meet safety, regulatory, and manufacturing requirements.
This position provides exposure to batch release processes, regulatory documentation, and pharmaceutical quality systems within a globally recognized healthcare company. Such experience can help professionals build strong careers in quality assurance, regulatory compliance, and pharmaceutical manufacturing operations. Associate I Quality Assurance Job at Baxter
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that publishes pharmaceutical and healthcare industry job updates for informational purposes only.
We do not conduct recruitment or charge any fees for job applications. Candidates are advised to verify job details directly on the official company website before applying. IndiaPharmaJobs.in is not affiliated with Baxter or any other company mentioned in this job posting. Associate I Quality Assurance Job at Baxter
Final Call-to-Action
Candidates interested in building a career in pharmaceutical quality assurance and regulatory compliance should consider applying for this opportunity. Submit your online application before the deadline and ensure your resume highlights experience in GMP compliance, batch documentation review, and quality investigations to improve your chances of being shortlisted for the Associate I – Quality Assurance role at Baxter. Associate I Quality Assurance Job at Baxter
