Research Associate Jobs at Piramal | Chemistry Graduates Apply
Are you looking for Research Associate Jobs with a globally trusted pharmaceutical organization? Piramal Pharma Solutions is hiring a Senior Research Associate to support analytical development activities while working in a world-class CDMO environment. This role offers hands-on exposure to advanced analytical instruments, method development, and regulatory-compliant laboratory practices, making it an excellent opportunity for professionals seeking long-term growth through Piramal careers.
About Piramal Pharma Solutions
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers 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, including the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics, including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private
Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.Job Description
To perform calibration of the analytical instruments as per the calibration schedule. Follow standard cGLP practices during lab experiments. Operation of HPLC, GC, Dissolution, FTIR, UV-Spectrophotometer, KF (Karl Fischer) Auto Titrator, and Auto Titrator. Cleaning verification method development. 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 submitting for review and release. Follow GxP (GMP, GDP, GLP) for all processes. Preparation of test procedures for routine development analysis.
Qualifications
M.Sc. in Analytical/Organic Chemistry. M.Pharm in Pharmaceutical Analysis/Quality Assurance/ Chemistry.
Required Skills
Operation of HPLC, GC, Dissolution, FTIR, UV-Spectrophotometer, KF (Karl Fischer) Auto Titrator, and Auto Titrator.
Job Info
- Job Identification: 10079
- Job Category: Analytical Development
- Posting Date: 12/24/2025, 08:18 AM
- Degree Level: Master’s Degree
- Job Schedule: Full-time
- Locations: Plot No. -19, PHARMEZ, Sarkhej-Bawala NH-8A, Ahmedabad, Gujarat, 362001, IN.
