Senior Research Associate - AD

piramalpharma; Ahmedabad District; On-site; INR 700,000 - 950,000; Full time

Job summary

Piramal Pharma Solutions in Ahmedabad is seeking a Senior Research Associate to perform routine analysis of formulation samples and support analytical activities.

The role involves calibrating analytical instruments, conducting stability studies, and documenting procedures under cGMP/GxP guidelines, with emphasis on accuracy and compliance. The candidate will contribute to method development and validation, ensuring quality data for release.

Qualifications

• Experience in analytical chemistry and GMP environments.
• Ability to perform calibration and method development.
• Exposure to stability studies and method verification.

Responsibilities

• Carry out routine analysis of formulation samples.
• Calibrate analytical instruments and review data.
• Support method development and validation activities.

Job description

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Division

Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Senior Research Associate - AD

Job Description

• Routine analysis of formulation samples
• Calibration of analytical instruments
• Stability study of lab batches
• Preparation of test procedure, development reports
• Review of routine analytical activities (Peer review)

• Routine analysis of formulation samples
• Calibration of analytical instruments
• Stability study of lab batches
• Preparation of test procedure, development reports
• Review of routine analytical activities (Peer review)

Job Description: It includes the job duties and responsibilities of the work

To perform calibration of the analytical instruments as per calibration schedule

Follow the standard practices cGLP during lab experiments

Cleaning verification method development and validation

API method evaluation and verification

API solubility study assessment

Method Development for drug product formulation

Routine analysis of development samples and lab stability samples

Method verification of different analytical methods

Reporting of analytical data and submit for review and release

ARF release of raw material and packaging material

Preparation of test procedures for routine development analysis

Follow in-house compliance system

Maintain hygienic condition in respective department

Column Management

TRF entries in common portal for tracking managment

Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements.

Follow GxP (GMP, GDP, GLP, DI) for all processes.