QC Executive Jobs in Gufic Biosciences Ltd - Indore, Madhya Pradesh

QC Executive Jobs in Gufic Biosciences Ltd - Indore, Madhya Pradesh

work outline icon2 - 8 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Gufic Biosciences Ltd.

time outline iconIndore, Madhya Pradesh, India

Posted on 11-03-2026

1 Vacancy

Description

  • Job Title: QC Executive
  • Qualification: BPharm
  • Location: Gufic Biosciences Ltd - Indore, Madhya Pradesh
  • Work Experience: 2 to 8 Years

Job Description

  • Perform QC testing of raw materials, in-process samples, and finished products.
  • Ensure all testing follows SOPs and GMP guidelines.
  • Maintain laboratory records and batch test reports accurately.
  • Report deviations or discrepancies to QC/QA Manager.
  • Assist in environmental monitoring and calibration of instruments.
  • Participate in internal audits and support external audits if needed.
  • Follow safety guidelines in the laboratory and production areas.
  • Coordinate with Production and QA for smooth workflow.
  • Support QC Manager in daily laboratory operations.

Take this opportunity to join Gufic Biosciences Ltd - Indore, Madhya Pradesh as a QC Executive in Indore, Madhya Pradesh 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 Control (QC)

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

Attention to DetailTeam working SkillsBasic Computer KnowledgeCoordination Skills

About Organization

Gufic Biosciences Ltd is a leading pharmaceutical company engaged in manufacturing active pharmaceutical ingredients, generic medicines, and lyophilized injectable products for global markets. The company operates advanced manufacturing facilities and follows strict regulatory and quality standards in pharmaceutical production. The role involves performing quality control testing of raw materials, in-process samples, and finished products. Responsibilities include maintaining laboratory documentation, following GLP and GMP guidelines, and ensuring product quality compliance. The position focuses on accurate testing, regulatory compliance, and maintaining high pharmaceutical quality standards.

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