5 Reference Standards Jobs

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 Qualifications Required: - Degree in Chemistry, Biochemistry, or related field - Experience with analytical instruments like HPLC - Strong attention to detail and accuracy in documentation Please note that this is a full-time position with the requirement to work in person at the specified work location.,

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 sheets, as well as master lists of instruments and equipment, along with their respective Qualification documents. Furthermore, you will play a crucial role in reviewing Preventive Maintenance and Calibration schedules, along with the Calibration data of all Analytical Instruments housed within the Quality Control laboratory. You will also be tasked with reviewing Method transfer/verification/validation protocols and reports, including the raw data, as well as evaluating Reference Standards/Working Standards and their respective Certificates of Analysis. In order to ensure the consistency of analytical trends, you will be expected to prepare quality comparison sheets for all dispatched materials. Your role will also involve reviewing monthly comprehensive assessment reports, laboratory errors, invalidations, and Analyst Qualification raw data. Additionally, you will need to conduct an audit trail review of all standalone instruments and Empower systems within the Quality Control department, as well as reviewing certificate of analysis documents. Key Competencies required for this role include excellent verbal and written communication skills, persuasiveness, strong inter-personal skills, adaptability, foresight, and a solid understanding of business processes. If you possess these competencies and are ready to take on the responsibility of maintaining quality standards within the laboratory, we encourage you to apply for this position.,

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 to maintain and archive relevant data in accordance with Standard Operating Procedures (SOPs) in coordination with the QC associate. The ideal candidate for this position should hold a B.Pharm or B.Sc. in Lifescience and possess 0-6 years of relevant experience. Strong attention to detail, organizational skills, and the ability to work effectively in a team are essential for success in this role.,

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.,

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.,