Claris Lifesciences Limited

Ahmedabad, Gujarat

Company details

Industry:
Manufacturing
Number of workers:
1500
Website:

Company Description


Claris Lifesciences is an Indian sterile injectables pharmaceutical company with a market presence across 100 countries worldwide. We primarily manufacture and market products across multiple markets, and therapeutic segments. A significant majority of these products are generic drugs that are capable of being directly injected into the human body and are predominantly used in the treatment of critical illnesses.

Claris Lifesciences Limited

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job postings

  • To execute and review internal audits for the organization, including follow-up audits; assisting in undertaking special reviews, as per applicable guidelines and schedule. Responsibilities To conduct internal control evaluation for identifying process & control gaps; and ensure that objectives of the organization are achieved economically, efficiently, and effectively. To undertake periodic reviews and ...

  • Performing month closing activity of CO Cycle run and WIP Calculation and its JV Posting there in System and Actual Price Valuation, Reviewing the Adj. entry for Expiry product write offs. Preparing and presenting variance analysis and exception reports showing the difference in Standard Cost and Actual cost and all the parameters affecting product costing like (Landing prices of Component material ...

  • To be responsible for sourcing, executing, and working on due diligence of venture capital transactions to build a portfolio To identify investment opportunities as well as provide operational support to the portfolio companies To identify the potential clients and build a steady pipeline of new prospects with proactive strategies To identify any new investment opportunities based on market and ...

  • To prepare manpower and hiring budget in line with business planning. To prepare hiring plan based on manpower planning along with the HOD and formulate action plan with team members for achieving the targets. To see that the stakeholders expectations are meeting by filling up the open positions within defined timeline in line with the budget decided. To suggest improvisations by finding new avenues ...

  • Thorough understanding & work experience of - Environmental Monitoring - Sterility, Bacterial Endotoxin Test - Micro Validation - Plates & Tube Observation and - Trending. Key responsibilities & authorities : > To prepare the media, as and when required. > To observe the tubes and plates and to supervise the discarding method of the same. > To perform periodic microbiological tests as per the schedule, as per Standard ...

  • Must have experience in injectable production/ manufacturing & regulated plant. To do on line operation checking and ensure online entries in Batch Manufacturing Record (BMR), log books & related documents as per Standard Operating Procedure (SOP) To supervise manufacturing activities i.e. sterilization, mixing, filling in allocated shifts and ensure process adherence as per standard operating procedure (SOPs) To ...

  • Desired Experience: > 3 - 4 Years of experience in Quality Control (IPPT, Finished Product, Batch Release, Analytical Method Transfer, Retain Sample, Raw Material & Packing Material) in Injectables / Parenteral manufacturing facilities. Functional Expertise: > Thorough understanding of Testing & Sampling of Raw Material & Packing Material, Finished Products, GLP, GMP, OOS, Batch Release, Analytical Method Transfer, Retain ...

  • To actively participation during successful technology transfer of products from R&D to various manufacturing locations To verify the technology transfer documents issued from F&D/ADL for adequacy and accuracy. Responsible for scale-up and identification of critical process parameters in consultation with F&D Prepare and review scale up reports based on the optimization batches clearly ...

  • - To do the Analytical method development and validation for API and finished product by HPLC and GC. - Responsible for Analytical method transfer activity - Working standard preparation and storage as per SOP - The person shall be responsible to prepare the SOPs, protocol and report for Stability Study, Essential Similarity (Stress and Unstressed), Specification and Method of Analysis of Raw Material, Packing ...

  • - Development of generic injectable Liquid and Lyophilized drug products for regulated and semi regulated markets. - Development of Anticancer and Immuno-suppressant drug products. - To take laboratory trials, stability batches and other product related studies and documentations of the same. - To do the literature work related to product development. - To identify the QTPP and CQAs from characterization of ...

  • - Development of generic injectable Liquid and Lyophilized drug products for regulated and semi regulated markets. - Development of Anticancer and Immuno-suppressant drug products. - To take laboratory trials, stability batches and other product related studies and documentations of the same. - To do the literature work related to product development. - To identify the QTPP and CQAs from characterization of ...

  • > To carry out the sampling of all the materials according to Standard Operating Procedure (SOP). > To carry out the testing of Raw Material and Packing Material according to approved procedure. > To release Raw Material and Packing Material. > To carry out the calibration of instruments as per the schedule. > To prepare the working standards as per the guidelines and various pharmacopoeias. > To ensure the status ...

  • > To prepare the media, as and when required. > To observe the tubes and plates and to supervise the discarding method of the same. > To perform periodic microbiological tests as per the schedule, as per Standard Operating Procedure (SOP). > To perform the Bacterial Endotoxin Test as per the schedule. > To test the material for their pre-sterile bio-burden and to test Raw Material (RM)/ Packing Material (PM) for ...

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