Analyst

Softgel Healthcare

Tamil Nadu

On-site

INR 420,000 - 640,000

Full time

14 days+

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Job summary

Softgel Healthcare in Tamil Nadu is seeking an analytical chemist to develop and validate HPLC-based methods for pharmaceutical products. The role emphasizes method transfer, validation, and regulatory compliance.

You will work with cross-functional teams to optimize processes, document experiments and results, and ensure GLP/cGMP adherence. A B.Pharma or B.Sc degree with 1–5 years' experience is required.

Qualifications

  • 1-5 years of experience in Analytical Method Development & Validation (HPLC) in pharma industry.
  • Bachelor's degree in B.Pharma or B.Sc from a recognized university.
  • Strong understanding of GLP, cGMP, and Quality Control principles.

Responsibilities

  • Develop analytical methods for pharmaceutical products using HPLC techniques.
  • Conduct method validation, transfer, and maintenance to ensure regulatory compliance.
  • Collaborate with cross-functional teams to resolve method-related issues and improve process efficiency.
  • Design and execute analytical research projects to develop new methods or optimize existing ones.
  • Ensure accurate documentation of all experimental procedures, results, and conclusions.

Skills

Analytical Method Development
HPLC
Validation

Education

B.Pharma or B.Sc

Job description

Roles and Responsibilities
  • Develop analytical methods for pharmaceutical products using HPLC techniques.
  • Conduct method validation, transfer, and maintenance to ensure compliance with regulatory requirements.
  • Collaborate with cross-functional teams to resolve method-related issues and improve process efficiency.
  • Design and execute analytical research projects to develop new methods or optimize existing ones.
  • Ensure accurate documentation of all experimental procedures, results, and conclusions.
Desired Candidate Profile
  • 1-5 years of experience in Analytical Method Development & Validation (HPLC) in Pharma Industry.
  • Bachelor's degree in B.Pharma or B.Sc from a recognized university.
  • Strong understanding of Good Laboratory Practices (GLP), Current Good Manufacturing Practice (cGMP), and Quality Control principles.
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