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10.0 - 14.0 years
0 Lacs
solapur, maharashtra
On-site
As a Quality Control Manager in the pharmaceutical industry, your primary responsibility will be to plan and execute Quality Control (QC) activities in a timely manner. You will need to ensure adherence to quality and safety norms, assess and organize required resources, and demonstrate good communication skills. Your role will be crucial in upholding cGMP guidelines and FDA standards. To excel in this position, you should possess excellent organization, time management, and leadership skills. A deep understanding of Bulk drugs and intermediates quality control processes and systems will be essential. You must also have comprehensive knowledge of quality control management, risk management, and safety regulations, along with a strong grasp of GMP principles and OH&S requirements. Your proficiency in documentation and audit requirements will be key to maintaining quality standards. Effective communication skills and the ability to build strong working relationships across the organization are essential. You should be confident, possess good decision-making abilities with attention to detail, and be well-versed in computer applications such as Word, Excel, PowerPoint, and Thunderbird. As a team player, you are expected to be proactive, focused, disciplined, and well-mannered. Being open to taking on additional responsibilities and demonstrating enthusiasm to work in a dynamic environment will be beneficial. Clear and concise communication is crucial for success in this role. Compliance with FDA approval and having prior experience in Quality Control as a Manager, Deputy Manager, or Assistant Manager are mandatory requirements for this position. The role is based in Solapur, Maharashtra, and requires a minimum of 10 years of total work experience. If you meet the specified criteria and are interested in this full-time, permanent position, kindly send your CV to vivekr@devichemscience.com.,
Posted 2 days ago
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