QC Executive Jobs in Glenmark Life Sciences Limited (GLS) - Indore, Madhya Pradesh

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QC Executive Jobs in Glenmark Life Sciences Limited (GLS) - Indore, Madhya Pradesh

work outline icon4 - 9 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Glenmark Life Sciences Limited (GLS)

time outline iconIndore, Madhya Pradesh, India

Posted on 16-04-2026

1 Vacancy

Description

  • Job Title: QC Executive
  • Qualification: BPharm/MPharm
  • Location: Glenmark Life Sciences Limited (GLS) - Indore, Madhya Pradesh
  • Work Experience: 4 to 9 Years

Job Description

  • Plan and execute stability studies as per ICH guidelines and approved protocols.
  • Perform analysis of stability samples using instruments such as HPLC, GC, UV-Visible Spectrophotometer, etc.
  • Monitor and maintain stability chambers for temperature and humidity conditions.
  • Record, review, and trend stability data to identify any changes in product quality.
  • Prepare stability protocols, reports, and summary documentation.
  • Investigate Out of Specification (OOS) and Out of Trend (OOT) results.

Take this opportunity to join Glenmark Life Sciences Limited (GLS) - 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

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Attention to DetailTeam working SkillsProblem SolvingCommunication Skills

About Organization

Glenmark Life Sciences Limited (GLS) is a pharmaceutical organization engaged in the development and manufacturing of high-quality active pharmaceutical ingredients (APIs) with a strong focus on regulatory compliance, product quality, and global standards. The role involves working in a manufacturing or operational environment to support production processes and ensure adherence to industry regulations. 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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