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Salary
≈ $9.5k – $23k per year (Estimated)
Location
In office (India)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 1, 2026. First seen by Alion on May 6, 2026. Par Health scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Par Health is a US pharmaceutical company based in Saint Louis, Missouri, that makes generic and essential medicines, including sterile injectables, controlled substances, active pharmaceutical ingredients and oral products for hospitals, pharmacies and distributors. It was formed from the generics businesses of Endo and Mallinckrodt after the two companies combined in 2025, and it runs manufacturing and research sites in Missouri, Indiana, Illinois, North Carolina, Pennsylvania and India. Par Health hires production and packaging operators, quality control technicians, research associates, compliance specialists, supply chain and EHS managers and sales staff.

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 timely

To 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 preparation

To Analysis and documentation of Reference standard samples as per MTH

To 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 environment

To support for Calibration/Preventive maintenance of all analytical instruments

Review of all executed analytical documents.

Maintenance for HPLC /GC Columns.

To perform Partial validation, Holding study, DMF queries and physiochemical studies

Responsibility for QMS system like Change control, Deviation and CAPA and related to QMS.

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