Research Associate
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Before you apply
LocationIndia - Alathur
Work modeon-site
SeniorityEntry
Experience1–2 yrs
Company size1,001–5,000 people
PostedJul 1, 2025 · 1y ago
Verified live1d ago
May no longer be actively hiring
Posted by the company on Jul 1, 2025
At a glanceSummarised by Seekless from the posting.
1 to 2 years' experience
post-graduation in Chemistry
analytical support for impurity and nitrosamines synthesis and qualification
analytical method development
routine analytical support for allotted project
qualification standards and control for allotted projects
support externals and internal (PD Lab work) queries
support nitrosamine and impurity qualification
daily calibration, document control and compliance
support queries for allotted project (API) timely
good housekeeping and adhere to GLP/cGMP norms in ARD Lab
cleanness of analytical instruments and working area and update all tag
analyze RM, in process, Intermediate and API in time
develop suitable analytical method and make STP in time
perform partial validation, Holding study, DMF queries and physiochemical studies
support stability sample analysis as per schedule
ensure completion of documents & data integrity and regulatory environment
Job Description Summary
This role requires 1 to 2 years’ experience. with post-graduation in Chemistry. This job will involve in Analytical support for impurity and nitrosamines synthesis and qualification.
Job Description
•
Analytical Method Development, Routine Analytical Support for 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 allotted project (API) timely
•
To ensure good housekeeping and adhere to GLP/cGMP norms in ARD Lab.
•
To ensure cleanness of analytical instruments and working area and update all tag.
•
To analyze RM, in process, Intermediate and API in time.
•
To develop the suitable analytical method and make STP in time.
•
To perform Partial validation, Holding study, DMF queries and physiochemical studies.
•
To support stability sample analysis as per schedule.
•
To ensure completion of documents & data integrity and regulatory environment.