Senior Research Associate-AD

Piramal Pharma Ltd; Ahmedabad District; On-site; INR 600,000 - 900,000; Full time

Job summary

Piramal Pharma Solutions, a CDMO in Ahmedabad, is seeking a Senior Research Associate-AD to perform routine analysis of formulation samples and calibration of analytical instruments in a GMP-compliant lab.

You will conduct stability studies, prepare test procedures, develop reports, and review routine analytical activities while ensuring traceability and adherence to EHS and GxP requirements.

Qualifications

• MSc in a relevant science discipline.
• Laboratory analytical skills preferred.

Responsibilities

• Routine analysis of formulation samples.
• Calibration of analytical instruments.
• Stability study of lab batches.
• Preparation of test procedures and development reports.
• Review of routine analytical activities (Peer review).
• Document reporting of analytical data and submission for review and release.
• Follow GxP (GMP, GDP, GLP) for all processes.

Education

Master of Science (MSc)

Job description

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

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)

• To perform calibration of the analytical instruments as per calibration schedule
• Follow the standard practices cGLP during lab experiments
• Cleaning verification method development
• API method evaluation and verification
• API solubility study assessment
• Column numbering and management
• Area and Milli-Q monitoring
• 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
• TRF entries in common portal for tracking management
• Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements.v Follow GxP (GMP, GDP, GLP) for all processes.

Master of Science (MSc) (Inactive)