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Ability to manage shift plans for formulation activities. Operate and maintain equipment such as autoclaves and blending vessels CIP and SIP skids. Ability to manage shift plans for filling activities. Operate and maintain equipment such as a Vial Washer, Tunnel Sterilizer, filling and Capping Machine.

Support to reaction monitoring, scale up and final analysis of samples as per monograph, in-house procedures including method development if required. Prepare development reports for Synthetic Support projects. Involve in project acceptance. Execute projects per the approved test protocols if assigned.

B.Pharm, B.Sc, M.Sc. OSD - Coating, Compression, Granulation, Ointment-External Preparation General Manufacturing and Sterile Manufacturing. IPQA - OSD and Injectable, AQA, APQR, Documentation, Validation, QMS, CQA, Artwork. Injectable, Aseptic, SIP, CIP, Batch Manufacturing, Bulk Manufacturing, Dry Powder, Oral Liquid. HPLC Operating, Dissolution, Assay

Analytical Method Development, Validation, Transfer activities of test like Assay, RS, Dissolution and Solvent. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule.

Method transfer of Pharmaceuticals Products and Materials. Analysis of In-process, Finished products, Stability study samples and raw material. Sampling and testing of Raw Materials, Packaging Materials and Water samples. Calibration and Handling of Laboratory Instruments like - GC, HPLC and Autotitrator etc

ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.

Finecure Pharmaceuticals Limited and its subsidiaries are leading manufacturers and marketers of Pharmaceutical formulations and Nutraceuticals in several therapeutic segments in dosage forms of Tablets, Capsules, Oral Liquids, Dry Syrup, Powders, Injections and Sachet.

Lincoln Pharmaceuticals Ltd., Ahmedabad based 40 years old, public limited having presence in 75+ countries, 1700+ registered products, own Manufacturing and R&D center and among india’s top 70 pharma company.

Responsible for monitoring and ensuring quality of products and comply with cGMP standards. Monitoring of critical process parameters, line clearance before batch initiation, verification of RM and equipment. In process sampling for quality check like pH, moisture content, and reaction monitoring.