Company Jobs

B.SC, B.Pharm, D. Pharma, with relevant experience in handling instrument i.e HPLC- Dissolution, GC, IR.UV, QC QMS, Material testing

Strong understanding of pharmaceutical formulations and patent law basics. Proficiency in patent databases and search strategies. Analytical mindset with excellent attention to detail. Good communication and technical writing skills.

Otsuka Pharmaceutical India Pvt. Ltd. is a fully-owned subsidiary of Japanese Company, Otsuka Pharmaceutical Factory, Inc, Japan. OPi deals in Infusion business in Indian and overseas markets. Any Science Graduate Fresher Or Any Non-Science Graduate Candidate having Min 2 Years of experience in Pharma Sales

B.Pharm/ M.Pharm ; Exposure to OSD Manufacturing operations like Compression, Pellet coating. Capsule filling, Primary Packing; Manufacturing / Packing Associate, Quality Control

M.Pharm, MSc; Knowledge in Complex Parenteral Ophthalmic drug product formulation development. Having tech transfer, plant batches execution experience

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.

Exercises good judgment on regulatory, quality, and technical related compliance issues. High personal integrity; trustworthy; strong compliance and quality mind-set. Solution orientated, strong sense of ownership and accountability.

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.

Perform real-time monitoring of production processes to ensure adherence to quality standards. Conduct routine inspections and in-process checks to verify compliance with specifications and protocols.

Review qualification protocols, reports, and documentation for accuracy, completeness, and compliance. Collaborate with cross-functional teams, including Quality Assurance, and Engineering, to ensure alignment and consistency in qualification practices.