51 Job openings found

1 Opening(s)
1.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below: To perform High Performance Liquid Chromatography analysis for various pharmaceutical tests including Related Substances, in compliance with 21 CFR Part 11 and cGMP guidelines. The role includes calibration, troubleshooting, integration, and data review activities related to HPLC.   Key Responsibilities: Perform routine and non-routine HPLC analysis for Assay, Related Substances, Content Uniformity, and other quality ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
0.00 LPA TO 3.60 LPA
  Develop, review, and update QA processes, checklists, and standard operating procedures (SOPs). Prepare and maintain quality documentation such as test plans, inspection reports, and audit findings. Conduct inspections, audits, and product tests (manual or automated depending on industry). Verify compliance with specifications, standards, and regulatory requirements. Identify, document, and track defects or nonconformities. Collaborate with ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
The Job description is as below: Blueprint Interpretation:Understanding technical drawings and specifications to create appropriate CNC programs. CNC Programming:Writing, editing, and optimizing CNC programs (often in languages like G-code) to control machine movements and operations. Machine Setup and Operation:Setting up CNC machines, selecting appropriate tools, and ensuring proper machine parameters. Quality ...
1 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.40 LPA
  Executing production activities as per approved Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOP). Monitoring production parameters such as temperature, humidity, and pressure during manufacturing.  Maintaining accurate records, including logbooks, BMR, and cleaning checklists. Conducting in-process checks to ensure quality standards are met at each stage of production. Coordinating with Quality Assurance (QA), ...
1 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.40 LPA
Perform microbiological assays, including cultures, staining, and identification of bacteria, fungi, and viruses under supervision. Assist in the preparation and sterilization of culture media, glassware, and laboratory equipment. Assist in testing samples. Keep the lab clean and organized, ensuring proper storage of microbiological specimens. Record and maintain accurate data on experimental results, including microbiological ...
1 Opening(s)
0 To 3.0 Year(s)
0.00 LPA TO 2.40 LPA
  Assist in testing raw materials, in-process samples, and finished products under supervision. Testing procedures like pH tests, viscosity, color tests, or basic microbiological tests depending on the industry. Accurately document test results and observations as per standard procedures. Familiarize yourself with the company's Quality Management System (QMS) for maintaining proper documentation. Maintain quality control ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
0.00 LPA TO 3.60 LPA
Daily accounting of the Purchase & Expenses Bills, Payments & Receipts. Records keeping for all type of vouchers and other works Good understanding on processes  Periodic Inventory verification  Bank reconciliations  Ledger reconciliation of Customers and Suppliers  Excel Knowledge and mail writing skills  General understanding of accounts matters  Handling routine Banking and Book Keeping Work Key Skills  Good communication Skills ...
1 Opening(s)
3.0 Year(s) To 12.0 Year(s)
0.00 LPA TO 6.00 LPA
Experience of working Europe Market is mandatory. Having worked US along with Europer will be added advantage. Identify market opportunities by understanding consumer needs, competitor analysis, and forecasting projected business.  Understand and navigate international regulations and compliance requirements for pharmaceutical products.  Developing and implementing strategies to launch and market products in global markets. Responsibilities can ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
0.00 LPA TO 3.60 LPA
 operates machinery to mix and granulate powdered ingredients, preparing them for tablet production.  Ensure proper cleaning and sanitization of equipment, monitor machine performance, and maintain records of production data.  Key tasks include weighing and measuring ingredients, operating mixing machines, and potentially drying or screening the granules.  starting and stopping the equipment, adjusting settings, ...
1 Opening(s)
2.0 Year(s) To 12.0 Year(s)
0.00 LPA TO 3.60 LPA
Operate and monitor the spray dryer and related machinery, ensuring efficient production.  monitor and adjust parameters like temperature, airflow, and feed rate, perform routine maintenance, and troubleshoot any operational issues. Maintain optimal drying parameters, including temperature, airflow, and feed rate, to achieve desired product characteristics.  Perform routine maintenance and cleaning of the spray ...

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