QA Officer Jobs in Stallion Laboratories Pvt Ltd - Ahmedabad, Gujarat
3 - 8 Years of Experience
Not disclosed 
Full TimeStallion Laboratories Pvt Ltd
Ahmedabad, Gujarat, India
Posted on 16-04-2026
1 Vacancy
Description
- Job Title: QA Officer
- Qualification: BPharm/MPharm
- Location: Stallion Laboratories Pvt Ltd - Ahmedabad, Gujarat
- Work Experience: 3 to 8 Years
Job Description
- Ensure compliance with GMP and quality assurance standards.
- Review batch manufacturing records and quality documents.
- Monitor production processes for quality compliance.
- Handle deviations, CAPA, and change control documentation.
- Conduct internal audits and quality inspections.
- Coordinate with QC and production teams for quality issues.
- Maintain QA documentation and quality records.
- Support regulatory audits and quality improvement activities.
Take this opportunity to join Stallion Laboratories Pvt Ltd - Ahmedabad, Gujarat as a QA Officer in Ahmedabad, Gujarat and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Functional Area
Pharma Quality Assurance (QA)
Preferred Education
Key Skills
About Organization
Stallion Laboratories Private Limited is a pharmaceutical formulation manufacturing organization focused on delivering high-quality medicines with a strong emphasis on regulatory compliance, product quality, and global standards. The company operates WHO-GMP, GLP, and ISO-certified manufacturing facilities and has a strong presence in both domestic and international markets, supplying products across multiple therapeutic segments. The role involves working in a manufacturing or operational environment to support production processes and ensure adherence to industry standards. Responsibilities include assisting in production activities, monitoring process parameters, maintaining accurate batch records and documentation, and ensuring compliance with safety, hygiene, and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to consistent product quality and operational efficiency.
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