Senior Research Associate-AD

Piramal Pharma Limited; Ahmedabad District; On-site; INR 600,000 - 800,000; Full time

Job summary

Piramal Pharma Solutions in India is seeking a Senior Research Associate in Analytical Development to support routine analysis of formulation samples, perform calibration of analytical instruments, and conduct stability studies on laboratory batches.

The role emphasizes adherence to cGxP guidelines (GMP/GDP/GLP), preparation of test procedures and development reports, and timely reporting of results for release and review.

Qualifications

• Experience in analytical development and quality systems.
• Familiarity with calibration and validation concepts.
• Understanding of GMP/GLP/GDP workflow and documentation.

Responsibilities

• Routine analysis of formulation samples.
• Calibration of analytical instruments.
• Stability study of lab batches.
• Preparation of test procedures and development reports.
• Follow cGLP and GxP (GMP, GDP, GLP) for all processes.

Skills

Analytical development

GxP compliance

Instrument calibration

Stability studies

Job description

Be the First to ApplyDivisionPiramal Pharma SolutionsPiramal 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.comJob TitleSenior Research Associate-ADJob DescriptionRoutine analysis of formulation samplesCalibration of analytical instrumentsStability study of lab batchesPreparation of test procedure, development reportsTo perform calibration of the analytical instruments as per calibration scheduleFollow the standard practices cGLP during lab experimentsCleaning verification method developmentAPI method evaluation and verificationAPI solubility study assessmentColumn numbering and managementMethod Development for drug product formulationRoutine analysis of development samples and lab stability samplesMethod verification of different analytical methodsReporting of analytical data and submit for review and releaseARF release of raw material and packaging materialPreparation of test procedures for routine development analysisFollow in-house compliance systemMaintain hygienic condition in respective departmentTRF entries in common portal for tracking managementEnsure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements.Follow GxP (GMP, GDP, GLP) for all processes.