Deputy General Manager-QA Jobs in Farmson Pharmaceutical Gujarat Pvt. Ltd - Vadodara, Gujarat

Deputy General Manager-QA Jobs in Farmson Pharmaceutical Gujarat Pvt. Ltd - Vadodara, Gujarat

work outline icon18 - 30 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Farmson Pharmaceutical Gujarat Pvt. Ltd.

time outline iconVadodara, Gujarat, India

Posted on 02-07-2026

1 Vacancy

Description

  • Job Title: Deputy General Manager-QA
  • Location: Farmson Pharmaceutical Gujarat Pvt. Ltd - Vadodara, Gujarat
  • Work Experience: 18 to 30 Years
  • Qualification: MSc Chemistry

Job Description

  • Lead and manage QA operations for DPI manufacturing lines, ensuring compliance with GMP, GLP, and regulatory guidelines (USFDA, EMA, WHO, MHRA).
  • Review, approve, and oversee Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and QA documentation for DPI products.
  • Oversee deviations, OOS/OOT investigations, CAPA, change controls, and risk management activities specific to DPI.
  • Monitor in-process checks, line clearance, and product release processes for inhalation products.

Take this opportunity to join Farmson Pharmaceutical Gujarat Pvt. Ltd - Vadodara, Gujarat as a Deputy General Manager-QA in Vadodara, 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

MSc Chemistry

Key Skills

Communication SkillsDocumentationTeam ManagementProblem Solving Skills

About Organization

Farmson Pharmaceutical Gujarat Pvt. Ltd. is a pharmaceutical manufacturing company focused on developing, manufacturing, and supplying high-quality Active Pharmaceutical Ingredients (APIs) and pharmaceutical 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, 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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