11 Shimadzu Jobs

Role & responsibilities 1. He shall be responsible to undertake training from the Section in Charge and the senior Analyst to make independent to carry out analysis. 2. He shall report to the senior analyst or analyst if any chemical, reagents or reference material is not available as per the requirement to carry out the analysis. 3. He shall be responsible to analyse samples received as per the specifications and for reporting of the results under the supervision of the senior analyst. 4. He shall be responsible to follow the quality system as per the policies laid down in the quality manual. 5. He shall be responsible for the preparation and standardization of the chemicals under the guidance of the senior analyst or analyst. 6. He shall be responsible to ensure proper documentation of all the data and its maintenance under the guidance of senior analyst or analyst. 7. He shall be responsible to follow the quality policies as per ISO/IEC17025, cGMP, GLP under the supervision of section In-charge or senior analyst. 8. He shall be responsible to perform all the chemical analysis. 9. He shall be responsible for operation, maintenance, timely calibrations of the following instruments: Weighing Balances pH and Conductivity Meter Melting Point Apparatus FTIR Instrument TOC Analyser Hot air ovens and Vacuum Oven Muffle furnace Disintegration Tester Dissolution Tester UV spectrophotometer Polarimeter Refractometer KF Auto titrator Melting point apparatus Tap density apparatus Friabilator

Department: Analytical Development Injectables / Complex Injectables US Market Job Description: Method Development of Drug Product and Method verification of Raw Materials using HPLC, UHPLC with sound knowledge of Chromeleon & Lab solution software. To perform analysis of Drug Product and Drug Substances for various test parameters and as per the product development requirement. Compilation of analytical results and preparation Method Development Report. Literature survey to support method development of Drug product and characterization activity of Drug product. Compilation and monitoring of routine and stability analysis data. Support to formulation team to develop the drug product.

Service Engineer - Bioanalytical @ Vimta Labs, Ltd, Cherlapally Experience: 6-10 years in relevant field CTC: Based on their current CTC; as per market standards Reports to: HOD Primary Responsibilities: Troubleshoot, repair, and maintain laboratory equipment, including LC-MS/MS, HPLC, Analytical Balances, pH Meters, Nitrogen Evaporators, Milli-Q Systems, Shakers, Deep Freezers (DF), Refrigerators, and other analytical instruments. Perform routine calibration, preventive maintenance, and performance verification of lab instruments to ensure compliance with regulatory standards. Diagnose and rectify hardware and software issues in analytical instruments and liaise with OEMs if required. Maintain proper documentation of service records, calibration logs, maintenance schedules, and equipment history as per GLP (Good Laboratory Practices). Ensure compliance with instrument qualification requirements (IQ/OQ/PQ) for all laboratory equipment. Train laboratory personnel on basic troubleshooting, proper handling, and best practices for maintaining lab instruments. Coordinate with vendors and service providers for spare parts, AMC (Annual Maintenance Contracts), and warranty-related issues. Maintain a log of breakdowns, repairs, and servicing activities for tracking instrument performance. Ensure adherence to laboratory safety guidelines while handling equipment and hazardous materials. Assist in laboratory audits and inspections by providing technical support and documentation. Secondary Responsibilities: Support installation and commissioning of new laboratory instruments. Ensure proper storage and maintenance of critical spare parts and consumables for laboratory instruments. Keep up to date with technological advancements and regulatory requirements in analytical instrumentation. Maintain workplace cleanliness and safety as per company and regulatory standards. Any other responsibility assigned by the HOD. Interested candidates can share their resumes to keerthana.rojanala@vimta.com Contact: Keerthana

Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

Position: QC Officer Qualification: B.Sc / M.Sc in Chemistry Experience: 3 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 4.5 Lacs per Annum. Location: Ankleshwar / Panoli. It's a Shift Working job Transport Provided. Industry: API PHARMA ONLY Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

Position: QC Executive Qualification: B.Sc / M.Sc in Chemistry Experience: 5 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 6.5 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API / Bulk Drugs / Pharma. Those working in Crop Sciences, Fertilisers are not eligible. Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

Analysis of different in process samples for Drying study Reaction monitoring by HPLC and other samples on GC Impurity profile and hold time study of process validation samples calibration activities reputed API industry having regulatory approvals

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Job Title: IT Lab Support Engineer (Off Role) Function / Role: Information Technology / Incharge Reporting to (position): IT Manager Role & responsibilities -Laborartory Support (21CFR part11 Compliance, Computer System Validation ) - Ensuring IT Software compliance and regulatory (ISO 27001:2022 \ USFDA \ NABL \ GAMP 5 \ GLP ) - Hands on Experience over Laborartory Process, Software and Documentation (ELN / SDMS / Chromeleon / GC / UV / Shimadzu / HPLC / FTIR /PSA). - Implement and manage various IT related initiatives taken up at AIL in the areas of ITAM, IT Security, IT Networking, software implementations related to IT, IT infrastructure and devices, Video Conferencing etc. at AIL location, in line with the IT roadmap. - Manage a team of 2-3 IT Engineers locally or remotely. Should have experience in Daily/Weekly Reporting and IT support team Management skills. - PR Creation in SAP and approvals including co-ordination with purchase and finance teams - Should be able to Manage IT Budgeting activities and IT Expense tracking against approved budgets - Implement, Manage and monitor IT Projects, MoCs (Management of Change) and Business projects related to plant location. - Project tracking, IT operations management and stakeholder management - Implement effective IT security systems on servers, network, user endpoints (laptops and desktops) and documentation to ensure security of data and applications in accordance to ISO 27001:2022 controls as per central team guideline - Coordination with Central team for management of Firewalls, switches, AV etc. - Implementation of SAM(Software Asset Mgmt) and ITAM/ISMS processes and applications at plant location in line with element guideline - Ensuring software compliance for all softwares being used at AIL site/plant locations. - implement various monitoring tools related to IT infrastructure, Log monitoring, IT Network and End user computing as per central team guideline - Manage and maintain change management as per IT Guidelines - Manage contracts for Network, Bandwidth, End-user Compute and other components in infrastructure/environment - Periodic review with vendors and ensure adherance of SLAs - New technology evaluation and implementation as per need of plant location - Design, develop and impart training content for IT related systems to users/IT team. - Proactively Plan and upgrade infrastructure as per business need - Good organizational and time management skills - Excellent communication and interpersonnel skills - Analytical thinker and problem solver

Ensures products meet quality standards & regulatory requirements by performing tests, Analyzing results & maintaining records, ensuring safe and effective medications. Must Exp in HPLC Instrument Like Agilent HPLC, Shimadzu HPLC, Agilent GC.

Key Responsibilities: Oversee and manage all laboratory activities, ensuring adherence to quality control standards. Perform and supervise GC and HPLC tests on gas calibration samples, ensuring accuracy and reliability of results. Ensure that all equipment in the QC lab is calibrated and maintained according to NABL guidelines and international quality standards. Lead the preparation, validation, and execution of standard operating procedures (SOPs) for QC testing. Ensure compliance with NABL accreditation requirements and maintain relevant documentation. Monitor the preparation of calibration gases and ensure quality control of calibration standards. Support the training and development of lab personnel on best practices for GC, HPLC, and calibration testing techniques. Prepare and review test reports, certifications, and quality documents. Assist in troubleshooting any laboratory equipment issues or test result discrepancies. Collaborate with cross-functional teams including R&D, production, and quality assurance to resolve technical issues and improve processes. Maintain inventory of lab consumables, chemicals, and equipment. Key Requirements: Bachelor's or Master's degree in Chemistry, Analytical Chemistry, or a related field. At least 5-9 years of experience in a QC laboratory, preferably in the gas calibration industry or a similar field. In-depth knowledge of GC and HPLC techniques, with hands-on experience in troubleshooting and running these instruments. Familiarity with NABL accreditation standards and quality assurance protocols. Strong understanding of gas calibration processes and relevant testing methodologies. Experience in preparing calibration standards and working with gas mixtures. Excellent problem-solving, organizational, and analytical skills. Strong communication skills to effectively report results and liaise with internal teams. Ability to supervise and mentor laboratory staff. Knowledge of lab safety protocols and environmental regulations.