Kesar Drugs Pvt Ltd

Industrial Area Phase I, Panchkula

Promote and sell pharmaceutical products to healthcare professionals.Develop strategic sales plans to achieve sales targets and company objectives.Establish and maintain relationships with key customers and healthcare professionals.Provide product information and answer customer inquiries.Analyze market trends and identify new business opportunities.Prepare regular sales reports and forecasts.Participate in sales meetings, conferences, and training programs.Monitor competitor activities and market conditions.

Must have knowledge of art work Documenting and reporting product or service quality levelsDeveloping and implementing standards for inspectionDeveloping a workflow for product inspectionDeveloping plans to help a company manage wasteCommunicating with other team members to solve problemsFollowing up with the appropriate channels when mistakes are foundTraining other quality insurance members on all inspection processes

Key Responsibilities:Maintaining IT infrastructure: This includes servers, networks, workstations, software, and hardware. The Assistant Manager will ensure these systems are functioning properly and provide support to users. Troubleshooting and problem-solving: They will diagnose and resolve IT issues, ensuring minimal disruption to plant operations. Managing IT projects: This may involve implementing new systems, upgrades, or other projects related to IT within the plant. Ensuring IT compliance: This includes adhering to industry regulations, security protocols, and company policies. Supporting end-users: Providing technical assistance and training to plant personnel. Collaborating with other teams: Working with plant maintenance, production, and other departments to ensure IT systems support their needs. Budgeting and resource allocation: May be involved in planning and managing the IT budget for the plant.

Performing HPLC Analysis: Running samples through HPLC instruments, interpreting results, and documenting findings. Maintaining Equipment: Ensuring HPLC systems are calibrated, maintained, and operating correctly. Method Development and Validation: Contributing to the development and validation of HPLC methods for various applications. Data Handling and Reporting: Managing raw data, compiling results, and generating reports as needed. Compliance with GLP/GMP: Adhering to Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) guidelines. Troubleshooting: Addressing any issues or problems that arise during HPLC analysis. Safety and Housekeeping: Maintaining a safe and organized laboratory environment. Documentation: Keeping accurate records of all analytical activities and data.

Ensuring all QC activities adhere to GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other relevant regulations. Maintaining accurate and complete QC documentation, including test reports, logs, and records. Participating in internal and external audits to ensure regulatory compliance. Supporting method validation, calibration, and equipment qualification activities. Testing and Analysis:Performing sampling, testing, and analysis of raw materials, in-process, and finished injectable products. Operating and maintaining laboratory instruments, such as HPLC, GC, UV, etc. Conducting stability studies to assess the shelf life of injectable products. Problem Solving and Improvement:Identifying and reporting deviations from quality standards, ensuring corrective and preventive actions (CAPA) are taken. Collaborating with production, QA, and other teams to resolve quality-related issues. Participating in the investigation of batch failures and OOS (Out of Specification) situations. Supporting the development and implementation of quality control systems. Supervision and Training:Supervising QC inspectors and ensuring they adhere to SOPs (Standard Operating Procedures). Providing training to QC staff on relevant procedures and techniques. Documentation and Reporting:Preparing and maintaining test reports, logs, and other QC documentation. Ensuring the timely completion and traceability of all testing activities. Maintaining accurate records of all QC data and results.