6 Proficiency Testing Jobs

As a diligent and detail-oriented Laboratory Supervisor, you will be responsible for overseeing the workflow to ensure optimal efficiency in testing processes and timely delivery of results. Your duties will include verifying quality control measures, such as validation of new reagents and other quality assurance activities, to uphold the performance of tests. It will be your responsibility to review and maintain records of test results and data archives, and ensure adherence to Infection Prevention and Control (IPC) procedures in the work environment. Your role will also involve evaluating proficiency testing and approving records, as well as reviewing and signing off on departmental standard operating procedures for clinical assays. Providing advisory services to patients, customers, and consultants on tests when necessary is a key aspect of this position. Participation in management review meetings, internal audits, and offering insights for continual improvement will be expected. You will be required to follow laboratory policies and procedures diligently, including proper attendance and time reporting. Additionally, managing mail communications of abnormal results and coordinating with public health departments or regulatory bodies will be within your purview. Ensuring that technicians comply with proper Bio-Medical Waste (BMW) management protocols, editing results as needed after retesting, and serving as a technical resource through staff training and participation in educational opportunities are essential responsibilities. You will be tasked with evaluating employees" competencies and providing guidance on the verification and implementation of new tests, kits, and instruments. Testing the virulence and strength of specific microbes to develop improved diagnostic and treatment methods, planning and organizing resources and activities, maintaining accurate records, and staying updated on new research findings and industry events are vital components of your role. Collaborating with colleagues from various departments, offering advice to medical staff and external bodies, and implementing preventive measures to curb the spread of infections in the laboratory are also part of your remit. Participating in quality improvement initiatives, reviewing critical values, interpreting and authorizing reports in Hematology and Clinical Pathology, and assisting in the recruitment of consultants as per approved requirements will be among your responsibilities. This is a full-time position that requires a minimum of 4 years of experience in Hematology. The work location is on-site, and your dedication and expertise will contribute significantly to the success of our laboratory operations.,

As the Manager-PRU Laboratory, your primary responsibility is to ensure compliance with safety rules and regulations, including the proper use of personal protective equipment (PPE), calibration, and training of manpower. You are expected to have a thorough understanding of PRU analysis for intermediate samples and final products, as well as knowledge of various product grades. Your duties also include monitoring the preparation of Standard Operating Procedures (SOPs), calibration, routine maintenance of instruments, and management of spares & chemicals inventory. Additionally, you will be responsible for safety protocols, external and internal audits, proficiency testing, in-house competency monitoring, and ensuring adherence to international standards such as ASTM, IP, UOP, ISO, BIS, APHA, etc. Your role involves highlighting any deviations from product specifications and assisting the Shift In-charge as needed, including taking on additional responsibilities when required. You will be accountable for new method/technology development, innovation/improvement in the lab, and ensuring the smooth functioning of the laboratory operations. In terms of team management, you will oversee the testing of intermediate and finished product samples, ensuring adherence to test methods, reliability of results, and timely validation in the Laboratory Information Management System (LIMS). You will also be responsible for instrument calibration, SOP preparation, documentation, and handling troubleshooting of instruments. Planning and budgeting, procurement of spares/consumables, and monitoring inventory will be part of your routine tasks. Your role extends to creating and implementing management frameworks to achieve targeted outcomes efficiently while complying with process design standards and statutory regulations. You will have the authority to make corrections in the analytical process, ensure timely report releases, and address any abnormalities or product failures promptly. Furthermore, your responsibilities include coordinating internally and externally for sample analysis, addressing customer complaints, providing feedback, and supporting customer developmental activities. You will also be accountable for implementing and improving Environmental Management Systems (EMS) and Occupational Health and Safety Management Systems (OHSMS) within the laboratory. Key challenges in your role include managing abnormal samples and results, ensuring instrument performance and calibration, maintaining inventory, troubleshooting instruments, and complying with NABL accreditation processes. You will be expected to make key decisions related to measurements, convey decisions to stakeholders, and recommend improvements in analytical practices and operations. Interdepartmental interactions, coordination with subordinates, area managers, external vendors, and customers will be crucial for successful laboratory operations. Your educational qualifications should include a B.Sc. or M.Sc. in Chemistry with at least 15 years of experience in PRU/Petroleum Refinery/Petrochemical laboratory settings. Additionally, you should possess functional skills in coordination, testing standards, LIMS, RIMS, IQCM, instrument handling, calibration, and troubleshooting, along with a sound understanding of product quality parameters and safety standards. Your behavioral skills should include team-building, result orientation, customer focus, operational excellence, and continuous learning and training abilities. In summary, as the Manager-PRU Laboratory, you play a vital role in ensuring the efficient and compliant operations of the laboratory, managing a team, maintaining quality standards, and driving continuous improvement in processes and procedures.,

The role involves taking responsibility for various activities related to sample characterisation. You will be tasked with testing using specified methods and standards, ensuring process compliance, maintaining quality assurance and control, and releasing reports. Additionally, you will be responsible for periodically assessing the uncertainty of measurement for identified parameters in the samples. Ensuring the completeness of all necessary information, records, documents, worksheets, standard operating procedures (SOPs), calibration schedules, preventive maintenance, proficiency testing (PT), and internal laboratory controls (ILC) will be a part of your role. Promptly handling equipment breakdown maintenance will be a key responsibility. Diligently following the ISO/IEC 17025:2017 system within the laboratory is essential. You will work under the supervision and guidance of the Assistant Laboratory Manager and report on daily activities and functioning. The candidate will require either a postgraduate degree in Engineering or Science, a graduate degree in Engineering or Science, a diploma in Engineering, an ITI certification in refrigeration, or a relevant field. You will need either 3-6 months or 1 to 3 years of experience in the testing field. This position is based in Ahmedabad. Remuneration will be as per industry standards.,

We are looking for experience Mep Site Engineer is responsible for overseeing the installation, maintenance, and repair of mechanical, electrical, and plumbing (Mep) systems on construction sites. They ensure these systems are installed according to design specifications, relevant codes, and safety regulations, while also coordinating with various stakeholders to maintain project timelines and resolve any on-site issues. managing Mep installations, ensuring they adhere to design drawings, specifications, and project schedules. conducting regular site inspections to monitor work progress, identify potential issues, and implement corrective measures. enforcing and promoting a safe working environment by ensuring compliance with health and safety regulations and company policies. staying updated on industry standards and regulations, ensuring all systems comply with applicable codes and requirements.

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.,

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.,