Walk-in Drive Vadodara 31st October - Formulation & Quality Control

Walk-in registration Link (Mandatory to fill) -

https://forms.cloud.microsoft/Pages/ResponsePage.aspx?id=ySOC_o5fXUiAkyTzx4edKPx_IzSh069JhfuIexoxHq1URDlJODQ5QzczQkhQN1pYMDY2UjNPUUY1Ui4u

FARD - Senior Executive:
Experience in analytical method Development, validation, method transfer, and regulatory filing support. Exposure to oral solid dosage forms (IR, ER, DR Tablets/Capsules). Experience with regulatory markets such as USFDA, EU, and ANVISA submissions.

FARD - Deputy Manager: Provide technical leadership by mentoring team members, overseeing laboratory operations, driving technology transfer activities, and managing analytical project deliverables within timelines. Strong exposure to analytical method validation/verification/transfer. IP/FP/Stability testing using LC/GC/Spectroscopy. (OSD & PFOS preferred) Well-versed in GxP/QMS & proficient in Empower, LIMS, Nichlon, QAMS, and DMS. Quality Control Develop and optimize sterile liquid and lyophilized injectable formulations. Conduct pre-formulation, compatibility, QbD/DoE, and stability studies. Execute lab, scale-up and exhibit batches; support technology transfer. Troubleshoot formulation and process-related issues. Prepare protocols, development reports, batch records, and regulatory documents. Coordinate with Analytical R&D, QA, QC, Manufacturing and Regulatory teams. Ensure compliance with cGMP, data integrity, and applicable regulatory guidelines. Understanding of QbD, DoE, scale-up, stability and container-closure systems. FRD (Injectables) - Senior Executive: Pharmacy Lead process scale-up from lab/pilot to commercial manufacturing. Optimize critical process parameters (CPPs) and material attributes (CMAs). Drive end-to-end technology transfer (TT), including dossiers and BMR/BPR preparation. Collaborate with manufacturing for engineering, exhibit, and validation batch.

MSAT - Executive / Senior Executive B.Tech / BE Chemical 3-5yrs