Research Associate, Analytical R&D

Paladin Labs Inc.; India; On-site; INR 600,000 - 900,000; Full time

Job summary

Paladin Labs Inc. is seeking a highly motivated analytical R&D chemist in India. The ideal candidate should have 2 to 5 years of experience in analytical chemistry and a postgraduate degree in Chemistry or Analytical Chemistry. Responsibilities include performing analytical method development and validation, supporting regulatory requirements, and ensuring adherence to GMP and GLP standards. The position offers an opportunity to work in a collaborative environment focused on continuous improvement and quality in healthcare.

Qualifications

• 2 to 5 years of experience in analytical chemistry.
• Knowhow of GMP operations and analytical instruments.
• Experience in method validation and development.

Responsibilities

• Ensure good housekeeping and adherence to GLP/cGMP norms.
• Perform analytical method development and validation in a timely manner.
• Support regulatory requirements as per committed timelines.
• Analyze raw materials, intermediates, and API samples.
• Maintain cleanliness of instruments and equipment.

Skills

Analytical method development

HPLC

GC

GCMS

IR

LCMS

Good Manufacturing Practices (GMP)

Good Laboratory Practices (GLP)

Analytical validation

Education

Post graduate degree in Chemistry or Analytical Chemistry

Job description

**Job Description Summary**We are seeking a highly motivated analytical R&D chemist to join our research and development team. We require 2 to 5 years’ experience and Post graduate chemistry/Analytical in developing and validating analytical methods for testing of API and release according to ICH and regulatory requirements. Having through knowledge of GMP operation and ability to work on Wet analysis and analytical instruments HPLC/GC/GCMS/IR/LCMS.**Job Description**To ensure good housekeeping and adhere to GLP/cGMP norms in ARD Lab and maintain cleanliness of instruments and equipment’s.To support and perform analytical method Development for each project timely.To support and perform analytical validation/Method transfer for each project timelyTo support regulatory requirement as per committed timeline.To provide analytical support related to production for sorting out issues, yield improvement and further optimizing the process as per schedule.To Sample/analyze RM,KSM, in process, cleaning, intermediate, stability and API and report preparationTo Analysis and documentation of Reference standard samples as per MTHTo support and perform analytical method development/Validation for EI by ICPMS and,IC,GCMS LCMS timely.To ensure completion of documents & data integrity and regulatory environmentTo support for Calibration/Preventive maintenance of all analytical instrumentsReview of all executed analytical documents.Maintenance for HPLC /GC Columns.To perform Partial validation, Holding study, DMF queries and physiochemical studiesResponsibility for QMS system like Change control, Deviation and CAPA and related to QMS.Come join us! At Par Health, we believe great healthcare is built on getting the essentials right.We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. *Elevating the Essentials* isn’t just our tagline, it’s the higher standard we live by every day.