Research Associate Jobs at Par Health | Chemistry Candidates Apply
Are you looking for rewarding Research Associate Jobs after completing your post-graduation in Chemistry? Here’s an excellent opportunity for professionals seeking MSc Chemistry Jobs and long-term growth in Chemistry Jobs within Analytical R&D. This Research Associate role in India – Alathur offers hands-on experience in analytical method development, impurity qualification, and regulatory compliance in a full-time position.
About Par Health
This organization operates in the pharmaceutical and analytical research domain, focusing on impurity profiling, nitrosamine qualification, API analysis, and regulatory compliance. With strong adherence to GLP/cGMP norms and data integrity standards, the company provides structured growth opportunities for professionals pursuing Research Associate Jobs, MSc Chemistry Jobs, and advanced Chemistry Jobs in Analytical R&D environments.
Job Title: Research Associate
- Locations: India – Alathur
- Time Type: Full-time
- Job Requisition ID: R002376
Job Description Summary:
This role requires 1 to 2 years of experience, with a post-graduation in Chemistry. This job will involve analytical support for impurity and nitrosamine synthesis and qualification.
Job Description:
- Analytical Method Development, Routine Analytical Support for the allotted project
- Responsible for qualification standards and control for allotted projects
- To support externals and internal (PD Lab work) queries
- To support Nitrosamine and impurity qualification.
- Responsible for daily calibration, document control, and compliance.
- To support the queries for the allotted project (API) in a timely manner
- To ensure good housekeeping and adhere to GLP/cGMP norms in ARD Lab.
- To ensure the cleanness of analytical instruments and the working area, and update all tags.
- To analyze RM, in process, Intermediate and API in time.
- To develop a suitable analytical method and make STP in time.
- To perform Partial validation, Holding study, DMF queries, and physicochemical studies.
- To support stability sample analysis as per the schedule.
- To ensure completion of documents & data integrity in a regulatory environment.
