185 Job openings found

? HPLC/GC Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as per defined test procedure.? Chemical Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as and when required.? Sampling of intermediate, finished product and raw material samples as and when required.? To maintain Raw ...

? HPLC/GC Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as per defined test procedure.? Chemical Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as and when required.? Sampling of intermediate, finished product and raw material samples as and when required.? To maintain Raw ...

B R AGROTECH LTD, PANOLI   Department :- Quality Control Designation- CHEMIST, SR. CHEMIST Min. Qualification- B.sc/M.sc (Chemistry) JOB RESPONSIBILITY Key Criteria: Candidate should minimum 3 years of Experience in Agrochemical / Pesticides (Herbicide, Insecticide, Fungicide)  products and their Formulations. Must be Knowledge of Kinds of Formulations  in Pesticides. Also should be Knowledge of Principles ,Guidelines ,Limitations ...

Sr.No. Job Description1. Registration and analysis of GP&T Lab samples.2. Documentation and analytical result reporting in LIMS.3. Daily calibration of GP&T lab instruments and documentation as per standardoperation procedure (Balance / Halogen moisture analyzer / pH meter / KF).4. Periodic calibration of PD lab instrument and documentation as per standardoperation ...

Must be m.sc/ M.pharma with 15-20 Year experience in commercial Lab Pharmaceuticals products Testing Responsible for ensuring the execution of all types of analytical activities (related to LC-MS/MS, GC-MS/MS, HPLC, GC, ICP-MS, Wet analysis, Microbiology) including planning, work allotment, analysis, trouble shooting and reporting of the performed work. Responsible for ensuring the optimum ...

Job Profile:- 1) Development and Stability profiling of Leachable check study. 2) Complete extractable check study of Container Closure System & leachable check study of finished product by HPLC and GCMS method. 3) Identification of unknown impurities and evaluation through toxicological assessment.  4) Performed schedule calibration of HPLC and GCMS

Position: QC Manager Location: Palanpur, Gujarat Industry: Pharma – API Key Responsibilities: Lead and oversee Quality Control operations in compliance with cGMP & regulatory guidelines. Manage QC documentation, including qc document review, SOPs, and analytical records. Supervise laboratory activities such as RM, PM, in-process, and finished product testing. Ensure timely calibration, qualification, and maintenance of ...

Position:          Research Associate Location:         Vadodara Experience:     3 - 5 Years Industries:       Pharma   Responsibilities: Synthetic Chemistry / Lab Work Perform multi-step organic synthesis of target molecules as per project requirements. Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products. Maintain accurate lab records and notebooks (ELN ...

Position:          ADL Executive Location:          Paria - Vapi Experience:      4 - 8  Years Industries:       Pharma   Responsibilities:- Develop and validate analytical methods for raw materials and finished products. Operate instruments like HPLC, GC, UV, IR, and dissolution testers. Prepare method validation protocols and reports as per ICH ...

Position:          Officer/Executive – RA Location:         Paria - Vapi Experience:     2 - 5 Years Industries:       Pharma   Responsibilities: Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil & Mexico), African, and EU regions. Handle full lifecycle of product registration including new submissions, renewals. Review technical documentation: ...