Research Associate

Paladin Labs Inc.; India; On-site; INR 300,000 - 500,000; Full time

Job summary

Paladin Labs Inc. is seeking a Research Associate in Alathur, India. The role involves analytical support for impurity and nitrosamine synthesis. Candidates must have 1 to 2 years of relevant experience and a post-graduate degree in Chemistry. Responsibilities include developing analytical methods, managing document compliance, and ensuring adherence to GLP/cGMP standards. The position emphasizes maintaining a clean and organized laboratory environment.

Qualifications

• 1 to 2 years' experience in analytical support.
• Ability to comply with GLP/cGMP norms in a laboratory environment.
• Experience in qualification standards and control for projects.

Responsibilities

• Conduct analytical method development and routine support for projects.
• Ensure timely completion of document control and compliance.
• Maintain cleanliness of analytical instruments and working area.

Skills

Analytical Method Development

Routine Analytical Support

Nitrosamine Qualification

Document Control

Education

Post-graduation in Chemistry

Job description

## Research AssociateApplylocations: India - Alathurtime type: Full timeposted on: Posted Yesterdayjob requisition id: R002660**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.