Manager/Dy. Manager-QA Jobs in Stallion Laboratories Pvt Ltd - Ahmedabad, Gujarat

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Manager/Dy. Manager-QA Jobs in Stallion Laboratories Pvt Ltd - Ahmedabad, Gujarat

work outline icon10 - 12 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Stallion Laboratories Pvt Ltd

time outline iconAhmedabad, Gujarat, India

Posted on 03-07-2026

1 Vacancy

Description

  • Job Title: Manager/Dy. Manager-QA
  • Qualification: Graduate
  • Location: Stallion Laboratories Pvt Ltd - Ahmedabad, Gujarat
  • Work Experience: 10 to 12 Years

Job Description

  • Manage and maintain the Quality Management System (QMS) as per GMP, GLP, ISO, and regulatory guidelines.
  • Review and approve SOPs, batch manufacturing records (BMR), batch packing records (BPR), and other QA documents.
  • Handle deviations, OOS (Out of Specification), change controls, and CAPA implementation.
  • Lead internal audits and coordinate external regulatory audits (FDA, WHO, MHRA, NABH, etc.).
  • Ensure data integrity and compliance with documentation practices.

Take this opportunity to join Stallion Laboratories Pvt Ltd - Ahmedabad, Gujarat as a Manager/Dy. Manager-QA 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

BPharm (Bachelor Of Pharmacy)

Key Skills

TeamworkDocumentationTime Management SkillRecord Keeping

About Organization

Stallion Laboratories Pvt Ltd is a pharmaceutical manufacturing company focused on developing, manufacturing, and marketing high-quality pharmaceutical formulations and healthcare products with an emphasis on innovation, regulatory compliance, and global quality standards. The role involves working in a professional pharmaceutical manufacturing environment to support production, quality assurance, quality control, research and development, documentation, and operational activities. Responsibilities include maintaining GMP compliance, handling manufacturing and quality records, coordinating with cross-functional teams, monitoring production and quality processes, and supporting efficient plant operations. The role also requires strong analytical skills, teamwork, adherence to regulatory guidelines, and commitment to delivering safe, effective, and high-quality pharmaceutical products and healthcare solutions.

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