HomeProductionExecutive - Analytical Method Development & Validation | Gujarat Liqui Pharmacaps |...

Executive – Analytical Method Development & Validation | Gujarat Liqui Pharmacaps | Vadodara

-

GLPL India is certified by ISO 9001: 2015 for Quality Management System, 14001:2015 for Environment Management System, 22000:2005 for Food Management System, and ISO/IEC 17025:2005 for Laboratory Management System. We are also a Star Export House Pharmaceutical Company having its state-of-the-art Soft-Gelatin Manufacturing facility at Waghodia, Vadodara, Gujarat, India. We have a comprehensive basket of innovative formulations in Pain Management, Anti-malarial, Anti-bacterial, Dietary Supplements, Multi-Vitamins and Herbals, and wide Domestic & International Business Network

Join Us for Regular Vacancy Updates on –

Join Our Telegram Group

Join Our Facebook Group

Our highly skilled global workforce, with their unwavering commitment to excellence, has been a critical pillar of GLPL success story. We achieve our shared goals and organizational objectives by strategically focusing on attracting, retaining, and developing the correct talent mix with diversity in relation to gender, age, expertise, and geographical heterogeneity.

Position: Executive – Analytical Method Development & Validation

Location: Vadodara, Gujarat, India

Job Description:

  • Setting up the Analytical Research & Development Laboratory as per the requirement of DGCI and MOH and generating necessary reports & documents.
  • Preparing various SOPs required for analytical method development & validation of developed method department (use of instruments) and follow Good Laboratory Practices (GLP).
  • Imparting training to team members regarding Instruments, Equipment use, and various quality control tests analysis method.
  • The literature search for Analytical Method Development for Assay, Dissolution, related Substance, Content of Uniformity, Forced Degradation Study, Viscosity, Impurities, and required other quality control tests for given products.

  • Sourcing new vendors for different required chemicals, columns, filters, etc. required for analytical method development, and analytical method validation for finished product and support to purchase for procurement of these items.
  • Preparing protocols and reports for analytical method development and analytical method validation for assay, dissolution, viscosity, impurities, and required other quality control tests for given products as per requirements of DCGI and various countries MOH, customers.
  • Performing analytical method development and validation for assay, dissolution, viscosity, impurities and required other quality control tests for given products as per requirements of DCGI and various countries MOH, customers
  • Handling routine analysis of Formulation department samples within a given timeline.
  • Performing various analytical tests and quality control troubleshooting
  • Completing different conditions, Stability Analysis within the timeline, and preparing Stability reports.
  • Handling Regulatory queries and preparing justification reports and risk analysis reports

Qualification: B.Pharma/M.Pharma

Experience: 2-7 Years

Salary: Negotiable

Contact Details:

Mr. Darpansinh Rajput

 hr1@glplindia.co.in, hr3@glplindia.co.in

Click for More R&D Jobs

Click for More Top Pharma Jobs


Join Us for Regular Vacancy Updates on –

Join Our Telegram Group

Join Our Facebook Group

LEAVE A REPLY

Please enter your comment!
Please enter your name here

- Advertisment -

Must Read