Quality Control (GC/ HPLC)

Urgent Requirement in PHARMA Industry...

Fresher's & Experience persons wanted in QUALITY CONTROL(Wet Analysis / HPLC / GC) AND RESEARCH & DEVELOPMENT (R&D) Department in Pharma Industry, Candidate should have good working experience in Pharma Manufacturing Units..

Roles and Responsibilities: FOR QC DEPARTMENT

In the pharmaceutical industry, the Quality Control (QC) department is responsible for testing and analyzing raw materials, in-process materials, and finished drug products to ensure they meet safety, purity, and efficacy standards.

QC Wet Analysis Department (or Wet Chemistry Lab) is responsible for performing traditional, bench-top chemical tests on raw materials, in-process samples, and finished products to ensure they meet quality specifications and regulatory standards.

Gas Chromatography (GC) is a critical analytical technique used within the QC department to: analyze the chemical components of drugs, determine the purity of ingredients, and verify that the final product meets specifications for release.

In the pharmaceutical industry, the Quality Control (QC) HPLC department uses High-Performance Liquid Chromatography (HPLC) to analyze raw materials, intermediate products, and final drug products, ensuring their identity, purity, potency, and stability.

Roles and Responsibilities: For R&D DEPARTMENT

The pharmaceutical R&D department is responsible for the entire lifecycle of new drugs, from discovering and developing them, through preclinical and clinical trials, to regulatory approval, manufacturing, and post-market surveillance. Key responsibilities include, conducting scientific research, designing experiments, analyzing data, managing clinical trials, ensuring regulatory compliance, and fostering innovation to bring safe and effective new treatments to patients.

Qualification: B.SC(CHEMISTRY) / M.SC(CHEMISTRY)

Experience: 0-5Years

Salary: 15-30K

Location : Jeedimetla ,Bollaram Hyderabad.

Note : Only Male Persons Required.

Contact: 8977333658.