On-site Application Chemist Toshvin Analytical

6.0 - 10.0 years

0 Lacs

maharashtra

On-site

As an On-site Application Chemist at Toshvin Analytical, you will play a crucial role in providing post-sale customer support on GCMS-MS applications. Your primary responsibility will involve visiting customer sites on a daily basis or being stationed at one customer location for a period of 6 to 12 months anywhere in India. In this role, you will support customers in method development, optimization, and validation activities related to their sample matrices. Your expertise in troubleshooting customer application issues and demonstrating advanced software capabilities will be essential. You will be expected to collaborate with the local application lab principals to address any unresolved customer application requests. Additionally, conducting application training sessions for customers" chemists to ensure effective utilization of the system and software will be part of your responsibilities. You will also prepare detailed application support reports and deliver PowerPoint presentations to customers as needed to communicate the activities carried out and results achieved. To excel in this role, you should have 6-8 years of experience in Pharma/Testing Lab/Food Testing Lab, with hands-on experience in TQMS, preferably with Shimadzu equipment. Your background should include expertise in analytical method development (AMD) activities, method development & validation protocols, proficiency testing requirements, and knowledge of existing regulations in Pharma/Food/EU Norms/Codex Test Methods. A minimum qualification of B.Sc. in Organic Chemistry or Analytical Chemistry is required, while an M.Sc. or equivalent post-graduation in Organic/Analytical Chemistry is preferred. Key Success Behaviours for this role include proficiency in handling chromatography sampling techniques such as Headspace Samplers, Thermal Desorption, Pyrolyzer, etc. Experience in analytical method development, optimization, and validation using these techniques is crucial. Familiarity with application workflows in relevant industry segments and knowledge of global regulations will be advantageous. Effective communication skills in English, both spoken and written, along with a willingness to travel extensively locally and outstation for customer support activities, are essential traits for success in this position. If you are a bright, motivated, and committed individual seeking a long-term career opportunity with one of the leading instrumentation companies in India, we encourage you to submit your CV to careers@toshvin.com. Join our team of experienced professionals at Toshvin Analytical, where growth meets opportunity.,

Posted 1 day ago

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Lab Supervisor Lupin Diagnostics

8.0 - 12.0 years

0 Lacs

bhubaneswar

On-site

As a Senior Lab Technician based in Bhubaneshwar, you will be responsible for performing internal quality control procedures and daily QC checks, while maintaining quality documentation in accordance with lab policies and procedures. Your role will also involve conducting preventive maintenance and calibration of laboratory instruments and equipment as per the defined program. Additionally, you will provide training to Medical Technologists/Medical Lab Technicians on working with automated instruments and in-house standard operating procedures. It will be your duty to ensure the maintenance of laboratory raw data and computer databases, as well as appropriate quality documentation for Proficiency testing, data entry in EQAS software, and monitoring Quality Indicators. You will be expected to perform RCA-resolution of complaints and issues, along with monitoring and compliance with biomedical waste management procedures. Critical value reporting and read back confirmation will also be part of your responsibilities, along with daily testing of samples, report entry, verification, and interpretation. Other tasks include storage and discarding of samples as per the retention period, periodic review of reference range variations, outsource samples test management, LIS transition checks, and verification checks for new tests added on LIS. Troubleshooting equipment problems and coordinating with equipment engineers for issue resolution will also fall under your scope of work. Furthermore, you will need to follow the Turnaround Time (TAT) standards, publishing monthly Management Information System (MIS) reports on TAT and critical values. Your role will also involve clinical correlation of reports and communication, new test or kit validation and verification, and maintenance of reagent or kit stock. You will be responsible for microscopic examinations, patient data entry into the accession register, duty roster preparation for all other lab personnel, and intra-lab test costing. Compliance with accreditation guidelines such as ISO 15189, NABL 112, and adherence to lab policies and procedures will be crucial aspects of your job. Finally, you will provide support during the launch of new labs or relevant setups. To apply for this position, please submit a detailed CV with the post applied for mentioned in the subject line.,

Posted 4 days ago

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