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