Trainee - R&D

Requirements

• Freshers or candidates with up to 1 year of experience in Analytical R&D / Quality Control laboratory are preferred.
• Analytical Instrumentation, Good Laboratory Practices (GLPs)

Benefits

Additional Information

Be the First to Apply 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 Trainee - R&D Job Description To execute analytical testing activities independently under the guidance of the supervisor, maintain laboratory documentation and records, and ensure cleanliness, safety, and compliance within the laboratory workplace Key Responsibilities Perform routine analytical testing activities as per approved procedures and test methods. Operate laboratory instruments such as HPLC, GC, UV, Dissolution apparatus, and other analytical equipment under supervision. Prepare reagents, standards, volumetric solutions, and sample preparations as per SOPs. Record analytical observations, raw data, and results accurately in laboratory notebooks and formats. Maintain proper documentation practices in line with GMP and data integrity requirements. Ensure calibration status and proper handling of laboratory instruments and glassware. Maintain cleanliness, safety, and housekeeping of the laboratory and work area. Follow laboratory safety procedures, EHS guidelines, and company policies. Support supervisors during method development, method validation, stability studies, and troubleshooting activities whenever required. Coordinate with cross-functional teams for sample receipt, analysis status, and documentation activities. Report deviations, incidents, or abnormal observations to the supervisor immediately. Educational Qualification M.Sc. in Chemistry, Analytical Chemistry

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