8 Shimadzu Jobs

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

Company: Strides Pharma Science Limited Department: Quality Control Profile: Executive Locations: Bangalore Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years Key skills: Analysis of Material / Product by referring current version of specification STP with relevant material code. Responsible for initial set up of Instrument/Equipment before starting the analysis with relevant online entries in usage Log / LIMS. Perform the Assay and RS by LC/UV/Dissolution, content uniformity by LC analysis with simple and complex products Tests as per SOP/STP. Proper handling of chromatographic column used for analysis. Maintain data integrity and appropriate traceability

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