Senior Executives for Quality Control

Role & Responsibilities (Quality Control)

HPLC Analysis of Solid Orals/Nasal Products

• You will perform High-Performance Liquid Chromatography (HPLC) testing on oral solid dosage forms (like tablets and capsules) and nasal products to ensure quality and consistency.

Hands-on Experience in Quality Control (QC) Activities

• You should be actively involved in day-to-day QC operations like sampling, testing, and documentation.

Key Sections (Work Areas)

IPFP (In-Process & Finished Products)

• Quality checks on products during and after manufacturing.

Nasal

• Specialized QC testing and handling of nasal dosage forms.

Raw Material

• Sampling and analysis of raw materials for identity, purity, and quality.

LCMS (Liquid Chromatography-Mass Spectrometry)

• Advanced instrumental analysis technique—used for detailed compound identification and impurity profiling.

Compliance with GMP/GLP Practices

• Work in strict adherence to

  Good Manufacturing Practices (GMP)

  and

  Good Laboratory Practices (GLP)

  to maintain regulatory and quality standards.

Experience Required: 2 to 7 Years

• Candidate should have relevant industry experience within the pharmaceutical sector, specifically in Quality Control.

Regulatory Plant Experience

• Prior work experience in plants approved by international regulators like

  USFDA

  (United States) or

  MHRA

  (UK) is preferred.
• This ensures familiarity with global standards and audit expectations.