Urgent opening For QC Analyst -HPLC (RM/PM/FG)

Intas

Ahmedabad District

On-site

INR 600,000 - 1,200,000

Full time

9 days ago

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Job summary

Intas is seeking a Quality Control professional to perform HPLC analyses on RM, PM and FG, and to prepare protocols, reports, and certificates of analysis. You will maintain records, calibrations, and ensure compliance with GMP.

The role requires 3-8 years in a QC lab with HPLC expertise and ability to collaborate with cross-functional teams to resolve quality issues. On-site in Ahmedabad.

Qualifications

  • MS/MSc in Science from a recognized university.
  • 3-8 years of experience in Quality Control Laboratory with HPLC expertise (RM/PM/FG).
  • Strong understanding of GMP guidelines and regulations in pharma.

Responsibilities

  • Conduct HPLC analysis of RM, PM, and FG to ensure quality standards.
  • Prepare protocols, reports, and certificates of analysis for RM/PM/FG.
  • Maintain accurate records of test results, calibration, and maintenance.
  • Collaborate with cross-functional teams to resolve product quality issues.
  • Ensure timely completion of tasks within deadlines.

Skills

HPLC Analysis
GMP Knowledge
Quality Control

Education

MS/MSc (Science) degree

Tools

QA reporting software

Job description

Roles and Responsibilities
  • Conduct HPLC analysis of Raw Materials (RM), Packaging Materials (PM), and Finished Goods (FG) to ensure compliance with quality standards.
  • Prepare protocols, reports, and certificates of analysis for raw materials, packaging materials, and finished goods.
  • Maintain accurate records of test results, instrument calibration, and maintenance schedules.
  • Collaborate with cross‑functional teams to resolve any issues related to product quality or contamination.
  • Ensure timely completion of tasks within the given deadlines.
  • MS/M.Sc(Science) degree from a recognized university.
  • 3-8 years of experience in Quality Control Laboratory with expertise in HPLC Analysis (RM/PM/FG).
  • Strong understanding of GMP guidelines and regulations governing pharmaceutical industry.
  • Proficiency in preparing protocols, reports, certificates of analysis using relevant software tools.
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