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GLP, Raw Material -Packaging Material, In Process-Finished Product, Method Verification Protocol preparation & Document Section Knowledge required; Water sampling/testing, EM Observation, Culture Handling, Media Management, Having Digital exposure for LIMS/ MODA Software B.Sc/ M.Sc/ B.Pharm; Lead QC operations as Shift In-Charge. Review analytical data, Ensure compliance with LIMS, GLP, ALCOA ICH/FDA

Delineating and characterizing the m6A RNA methylation marks in primary and relapsed B-cell Acute Lymphoblastic Leukemia; MSc Life Sciences research experience or PhD in life sciences; Hands on research experience in molecular biology experiments PCR, Real Time PCR, Cloning, bioinformatics analysis of transcriptomes, exomes, custom analysis is desirable.

Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable

M.Pharmacy / M.Sc. / BPharm; Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols.

M.Pharm / M.Sc; HPLC/GC/IC method development, feasibility, verification, equivalency, validation for API, complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated and India markets; Good understanding and hands on experience of analytical instruments like HPLC, IC, GC etc.

Emcure is fast-growing Indian pharmaceutical company engaged in developing, manufacturing, and marketing a broad range of pharmaceutical products globally.

Titan Laboratories Pvt.Ltd. is the one of select few Company in india with dedicated state of art WHO GMP facility for producing high quality Sustained and Modified Release Pellets, DC Granules& Taste Masked Granules.

Experience in regulatory strategy, dossier review, and submission for the US, EU, and Brazil markets. This role requires a deep understanding of CMC requirements and the ability to lead the regulatory strategy for various dosage forms, including complex injectables and ophthalmic products.