QC Analyst (GC) Jobs in CEPH Lifesciences Private Limited - Baddi, Himachal Pradesh

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QC Analyst (GC) Jobs in CEPH Lifesciences Private Limited - Baddi, Himachal Pradesh

work outline icon3 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

CEPH Lifesciences Private Limited

time outline iconBaddi, Himachal Pradesh, India

Posted on 08-04-2026

1 Vacancy

Description

  • Job Title: QC Analyst (GC)
  • Qualification: BPharm
  • Location: CEPH Lifesciences Private Limited - Baddi, Himachal Pradesh
  • Work Experience: 3 to 5 Years

Job Description

  • Perform analysis of raw materials, in-process samples, and finished products.
  • Operate analytical instruments such as HPLC, GC, UV, and dissolution apparatus.
  • Prepare reagents, solutions, and standardize volumetric solutions.
  • Record and maintain analytical data, test reports, and documentation.
  • Follow GLP, GMP, and laboratory safety guidelines.
  • Conduct calibration and routine maintenance of laboratory instruments.
  • Handle OOS (Out of Specification) and OOT (Out of Trend) investigations.

Take this opportunity to join CEPH Lifesciences Private Limited - Baddi, Himachal Pradesh as a QC Analyst (GC) in Baddi, Himachal 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

DocumentationAnalytical SkillsProblem Solving SkillsAttention to Detail

About Organization

CEPH Lifesciences Private Limited is a pharmaceutical organization engaged in the manufacturing of high-quality formulations with a strong focus on regulatory compliance, product quality, and efficient production processes. The role involves working in a manufacturing or operational environment to support production activities and ensure adherence to industry standards. Responsibilities include assisting in production operations, following Good Manufacturing Practices (GMP), maintaining accurate batch records and documentation, monitoring equipment performance, and ensuring compliance with safety and hygiene protocols. The role also requires coordination with quality assurance and quality control teams, adherence to regulatory guidelines, and maintaining consistency in product quality and operational efficiency.

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