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10.0 - 14.0 years
0 Lacs
ankleshwar, gujarat
On-site
As a Quality Control Manager at our company, your primary responsibilities will include overseeing the quality control department in Panoli, Gujarat. With over 10 years of experience and an educational background of M.Sc. in Chemistry, you will be leading the GC section and working standard section. Your duties will involve planning, distributing, and monitoring work in the GC section and working standard section. You will be responsible for tasks such as LIMS template preview, instrument method preparation, and updating in Empower software. Additionally, you will initiate laboratory events, out of specification instances, out of trend observations, deviations, and change controls in Track Wise, following standard operating procedures for investigations. It will be your duty to ensure the qualification of working standards, manage procurement activities for reference standards, impurity standards, GC standards, and GC columns. You will also oversee the cleanliness of instruments, workplaces, and laboratories, ensuring a safe environment by providing necessary personal protective equipment as per work requirements. Furthermore, you will be responsible for providing training to subordinates and adhering to safety protocols in the laboratory. You are expected to carry out any other activities as instructed from time to time to maintain the quality and efficiency of the quality control department.,
Posted 1 day ago
16.0 - 20.0 years
0 Lacs
ankleshwar, gujarat
On-site
You are being hired for the position of QC Head at our company based in Ankleshwar, Gujarat. As the QC Head, you will be responsible for ensuring the quality of all batches manufactured, overseeing the Quality Control department functions, and managing activities related to quality assurance. Your main duties will include sampling, inspection, and testing of raw materials, packaging materials, in-process products, and finished products as per specifications for release or rejection. You will also be in charge of stability chamber handling, stability testing, and evaluation of shelf-life of products, as well as preparing stability testing protocols and reports. In addition, you will conduct microbiological analysis of raw materials, finished products, water, and environmental bio-burden monitoring. You will review monthly trend reports for physicochemical and microbiological data and ensure compliance with predefined specifications. Analytical investigations for complaints, product recalls, out of specification results, and deviations will also fall under your purview. Furthermore, you will be responsible for internal Quality System audits, quality review, analysis of non-conforming products, reference standards, working standards, and solution preparations. You will plan and manage all activities of the Quality Control Department to assure the quality of all products manufactured by the company. Coordinating with the manufacturing department to control processes and products at every stage of manufacturing will also be part of your role. Moreover, you will work on the development of specifications and analytical procedures in coordination with the Quality Assurance Department and R&D. You will review the adequacy and relevance of specifications and analytical procedures, ensure instrument qualification, implement audit trail systems for data integrity and security, and coordinate technical audits of the Quality Control Laboratory. Your responsibilities will also include maintaining Quality Control records, control samples, release records, routine Good Laboratory Practices auditing, organizing training programs, establishing guidelines and procedures on cGMP and Good Laboratory Practice, and evaluating Change Control suggestions for overall reviews and validations. As the QC Head, you will play a key role in upholding quality standards, ensuring compliance with regulations, and contributing to the continuous improvement of quality control processes within the company.,
Posted 3 days ago
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