Jubilant Drug Discovery and Development Services (JDDDS), is part of the Jubilant LifeSciences family of companies with R&D Centers in India, USA and business offices in Asia, Europe and North America. JDDDS has a global reach and provides comprehensive drug discovery and development solutions from target discovery to clinical development in partnership with leading pharma companies worldwide.
With clear scientific focus in Oncology, Metabolic Disorders, CNS and Pain and Inflammation, JDDDS has rapidly emerged as a leading collaborator for pharma industry. In each of these therapeutic areas, Jubilant has developed a depth of expertise in discovery informatics, medicinal chemistry, structural biology, biology, in vitro, in vivo models and translational sciences. Combined with strong clinical development and manufacturing capabilities, Jubilant has emerged as a fully integrated company with end-to-end solution for pharma industry.
JDDDS business constitutes three Jubilant subsidiaries, Jubilant Biosys (Drug discovery services), Jubilant Chemsys (Chemistry services) and Jubilant Clinsys (Clinical trial services). With over 1200 highly skilled and experienced scientific and medical personnel spread across Bangalore and Noida in India, Europe and the US, the JDDDS vertical leverages the capabilities in emerging markets for a global outcome, accelerating the global drug development efforts.
Accountabilities Scope Of Work
Ensure the reliability of analytical data, result and report shall be as per regulatory compliance. Ensure effectively implementation & 100% adherence to ISMS, all statutory, regulatory, EHS compliance Operational excellence in procedure, practices and instrument's. Wet analysis (SOR, KF, LOD, ROI & FTIR). Daily & Monthly calibration (SOR, KF, pH, Balance& FTIR). Water validation
- Non Conformance & Observations
Calibration and maintenance of UV, GC, and HPLC, polarimeter, pH, balances and FTIR instrument as per defined procedure (SOP).
Maintain the time of analysis (TAT). TAT for GMP batch in-process analysis, for GMP intermediate and PR&D samples-
Ensure that All the Method Development for GC chromatography is completed on or before due date.
Ensure that All the analysis related to GC along with WET analysis (I.R, M.P., SOR, and K.F., U.V. LOD, Solubility,) and HPLC analysis (RXM, Cleaning, Assay and RS of daily or stability samples) of other project as required .
Monthly calibration of I.R., Polari meter, Balance & micro balance, pH, U.V, GC and perform water validation sampling & analysis.
