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Committed to Care and Cure, Gracure believes in Quality Products…On Time In Full. Keeping the vision of making world class affordable medicines Gracure is a research driven forward looking pharmaceutical organization with expertise in development of various finished dosage form. Gracure is an integrated pharmaceutical company engaged in Research and Development, Manufacturing, Sales and Marketing of Pharmaceutical Products. Our values and standards are the foundation of delivery of quality products in the International markets. Our values inspire us to grow continuously and meet demanding requirements of our partners.
Not specified
INR 7.0 - 10.0 Lacs P.A.
Work from Office
Full Time
Role & responsibilities a. Having experience for EB /PV data compilation and report preparation and review.b. Having experience for Executed document (BMR& BPR) review and compliance in coordination with validations requirement.c. Having exposure for hold time study data review and report compilation.d. Having exposure for sampling strategy of bulk and finished product in case of exhibit and commercial launch batches.e. Coordination with stability /micro/QC validation /production team for data collection and compliance as per validation requirement.f. Having exposure for QMS for validation recommendations closure and revision for routine commercials.g. Having exposure for document readiness and submission for product filing to regulatory department or client
Not specified
INR 7.5 - 11.0 Lacs P.A.
Work from Office
Full Time
Role & responsibilities a. Having experience for EB /PV data compilation and report preparation and review. b. Having experience for Executed document (BMR& BPR) review and compliance in coordination with validations requirement. c. Having exposure for hold time study data review and report compilation. d. Having exposure for sampling strategy of bulk and finished product in case of exhibit and commercial launch batches. e. Coordination with stability /micro/QC validation /production team for data collection and compliance as per validation requirement. f. Having exposure for QMS for validation recommendations closure and revision for routine commercials. g. Having exposure for document readiness and submission for product filing to regulatory department or client
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