Senior Research Associate-AD

Piramal Pharma Limited; India; On-site; INR 700,000 - 1,100,000; Full time

Job summary

Piramal Pharma Limited in India is seeking a Senior Research Associate-AD to conduct routine analysis of formulation samples and calibrate analytical instruments, ensuring cGLP compliance during lab experiments.

You will perform stability studies, prepare test procedures and development reports, review routine analytical activities, and participate in in‑house compliance systems, contributing to ARF material release and overall quality.

Qualifications

• Master of Science (MSc) in a relevant field.

Responsibilities

• Routine analysis of formulation samples.
• Calibration of analytical instruments.
• Stability study of lab batches.
• Preparation of test procedures, 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.

Education

Master of Science (MSc)

Job description

Company Overview

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

Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October2020, PPL received a 20% strategic growth investment from the Carlyle Group.

Job Title

Senior Research Associate-AD

Job Responsibilities

• 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

Qualifications

Master of Science (MSc) (Inactive)

EEO Statement

PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.