10 Reference Standards Jobs

As a Quality Control Laboratory Compliance Specialist, your role involves ensuring compliance with SOPs and regulatory requirements. Your responsibilities will include: - Imparting training to QC Associates on SOPs and current regulatory requirements based on review observations. - Reviewing Analytical data such as Finished, Intermediate, Raw material, and Stability. - Ensuring accuracy of analytical data by reviewing electronic data and sequence audit trail against hard copy. - Reviewing Stability Protocols, Stability schedules, and Stability data sheets. - Reviewing master list of instruments, equipments, and Qualification documents. - Reviewing Preventive maintenance schedules, Calibratio...

Role Overview: As a SolidWorks Drafting/Design Engineer, you will be responsible for working on Engineering Projects and carrying out drafting, modeling, and detail engineering. You will report to the Deputy Manager of Engineering. Key Responsibilities: - Prepare 3D models for parts, pipe routing, and support using SolidWorks software. - Create 2D detail drawings for machined components and assembly drawings. - Generate drawings and issue them in PDM (Product Data Management). - Develop Bill of Materials (BOM) in SAP with part coding system. - Ensure compliance with Armstrong Quality standards. Qualification Required: - Clear understanding of preparing detail drawings for manufacturing, cust...

As a Quality Control Analyst in the pharmaceutical industry, you will be responsible for sampling and analyzing a variety of materials including Raw materials, Packing materials, In process, Intermediate, and Finished products. Your role will also involve the calibration of all QC instruments, conducting Stability/Holding time studies, and handling Reference Standards while qualifying Working Standards. Key Responsibilities: - Sampling and analysis of Raw materials, Packing materials, In process, Intermediate, and Finished products - Calibration of all QC instruments - Conducting Stability/Holding time studies - Handling Reference Standards and qualification of Working Standards Qualificatio...

As a Quality Control Laboratory Compliance Specialist, your role will involve ensuring compliance with SOPs and regulatory requirements. You will be responsible for imparting training to QC Associates on SOPs and current regulatory requirements based on review observations. Your key responsibilities will include: - Reviewing analytical data for Finished, Intermediate, Raw materials, and Stability. - Ensuring the accuracy of analytical data by reviewing electronic data and sequence audit trail against hard copy. - Reviewing Stability Protocols, schedules, and data sheets. - Reviewing the master list of instruments, equipment, and Qualification documents. - Reviewing Preventive maintenance sch...

As a SolidWorks Drafting/Design Engineer at our company, your role will involve working on Engineering Projects and conducting drafting, modelling, and detail engineering. You will report to the Deputy Manager of Engineering. Key Responsibilities: - Prepare 3D models for parts, pipe routing, and support using SolidWorks software. - Develop 2D detail drawings for machined components and assembly drawings. - Create drawings and issue them in PDM (Product Data Management). - Generate Bills of Materials (BOM) in SAP with the part coding system. - Ensure compliance with Armstrong Quality standards. Key Requirements: - Possess a clear understanding of preparing detail drawings for manufacturing, c...

As a member of the team, you will be responsible for performing qualitative and quantitative analysis of raw materials, intermediates, and finished goods according to approved specifications, SOPs, and test methods. Your role will involve conducting testing using analytical instruments like HPLC and ensuring the accurate documentation of results in laboratory records. Key Responsibilities: - Perform qualitative and quantitative analysis of raw materials, intermediates, and finished goods - Conduct testing using analytical instruments such as HPLC - Prepare and standardize reagents, solutions, and reference standards for testing - Ensure accurate documentation of results in laboratory records...

As a Quality Control Laboratory Specialist, your primary responsibility will be to ensure compliance with Standard Operating Procedures (SOPs) and regulatory requirements within the laboratory. You will be required to provide training to QC Associates on SOPs and current regulatory standards based on review observations. Additionally, your role will involve reviewing a variety of analytical data including Finished, Intermediate, Raw Material, and Stability samples. It will be your duty to meticulously review electronic data and compare it with hard copies to guarantee the accuracy of the analytical results. You will also be responsible for examining Stability Protocols, schedules, data sheet...

As a Junior Research Associate in the Bioanalytical Research field, your responsibilities will include the operation and maintenance of various laboratory equipment. You will be required to handle biological samples, manage sample receipt and shipment, and procure biological matrix lots as needed. Additionally, you will be responsible for the operation, calibration, and maintenance of equipment such as deep freezers, refrigerators, Eurotherm, Thermo hygrometers, thermometers, centrifuge, evaporator, pH meter, balance, and pipettes. Furthermore, you will be involved in the management of biological samples including study samples, validation samples, and matrix lots. It will be crucial for you...

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 W...

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 m...