Intas Walk-In Drive for Quality Control – Reviewer, Analyst Positions

Intas pharmaceuticals recruitment notification

Intas Pharmaceuticals, a global leader in pharmaceutical formulation development, manufacturing, and marketing, is conducting a walk-in drive for Quality Control Reviewer and Analyst positions at Pharmez, Ahmedabad. If you have relevant experience and qualifications, don’t miss this chance to join a company committed to creating a world of good health, happiness, and hope.


Job Details

Department: Quality Control

Positions Available:

  1. Analyst (QC-FG/Stability/AMV)
    • Role: Officer to Executive
    • Qualifications: B. Pharmacy/M. Pharmacy/M.Sc./B.Sc.
    • Experience: 3-8 years
    • Key Skills:
      • Expertise in Finished, AMV, and Stability sections.
      • Proficient with instruments like HPLC and GC.
      • Knowledge of Chromeleon Software preferred.
  2. Reviewer
    • Role: Sr. Officer to Sr. Executive
    • Qualifications: B. Pharmacy/M. Pharmacy/M.Sc./B.Sc.
    • Experience: 6-12 years
    • Key Skills:
      • Strong knowledge of QC software, including HPLC, UV/IR, and LCMS.
      • Experience with LIMS, Chromeleon, and other laboratory software.
      • Familiarity with GDP/GLP/cGMP requirements.
      • Regulatory experience in USFDA, MHRA, TGA environments preferred.
Intas Walk-In Drive for Quality Control - Reviewer, Analyst Positions
Intas Walk-In Drive for Quality Control – Reviewer, Analyst Positions

Walk-In Interview Details

  • Date: Thursday, 12th December 2024
  • Time: 9:00 AM to 12:00 PM
  • Venue:
    Intas Pharmaceutical Limited
    Plot No. 05 to 14, Pharmez, Near Village Matoda,
    Sarkhej – Bavla Highway 8-A, Taluka- Sanand, Dist-Ahmedabad.

Responsibilities and Key Highlights

Analyst Position

  • Conduct quality testing of finished goods, AMV, and stability samples.
  • Operate advanced instruments such as HPLC and GC.
  • Ensure compliance with Good Laboratory Practices (GLP) and company standards.

Reviewer Position

  • Review audit trail data and ensure compliance with regulatory requirements.
  • Handle instruments like UV/IR, HPTLC, LCMS, and more.
  • Collaborate with cross-functional teams to maintain high standards of quality.
  • Provide expertise in regulatory frameworks like USFDA, MHRA, and TGA.

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