Role & responsibilities Preparation of annual Budgets and variance analysis reports Knowledge of preparing financial statements, Computation of Income Ability to understand and implement the finance processes and procedures GL Review Provisioning of expenses Payroll accounting and reporting Review and accounting of vendor invoices, travel reimbursements. Support for Statutory audit, Internal audit, Tax audit, Department audits, Due diligence Related party transaction reporting Statutory compliance reporting Preparation and filing of E-TDS returns under Direct tax provisions. Preparation of various reports as and when required by management. Qualifications & Experience Candidate should be a B.com/M.com graduate having 34 years of relevant experience. Self-starter, Exceptional communication skills. Well organized with ability prioritize activities Strong Commitment towards completion of work within timelines. Willing to take up Additional responsibilities as and when assigned by management. Candidate should be able to stretch as per the requirements of Management. Proficiency in Tally ERP & MS Excel
Role & responsibilities To perform Physico Chemical Parameters/Method development/Method Validation/Residue Studies/Stability studies /E-fate Studies. Strong knowledge, Handling and operations in analytical techniques, including HPLC, GC, FTIR, UV-VIS, LC-MS/MS and GC-MS/MS spectroscopy, etc. Preferable handling in LC-MS/MS and GC-MS/MS instruments. Develop and validate analytical methods for the analysis of various compounds using a variety of analytical instruments and along with troubleshooting. Understanding of regulatory requirements (OECD/EC/OPPTS/CIPAC/ASTM/SANTE/SANCO/EMA/ICH, etc.) and ensure compliance with GLP (Good Laboratory Practices) throughout the study process. Contribute to preparation of SOPs. Design and develop study protocols in accordance with regulatory guidelines and preparation of study reports. Investigate and solve analytical technical issues. Ready to work in Extra time/shift basis and independently. Preferred candidate profile
Role & responsibilities Ensuring GLP Compliance in the Department. Conduct of in vitro and in vivo genotoxicity studies (AMES, chromosomal aberration test, micronucleus test, mutation assay, COMET assay, Alternative studies) Plan and manage all departmental activities, including study scheduling, equipment maintenance, calibration, and procurement. Lead the team of scientists and ensure adequate staffing and smooth workflow. Prepare, approve, and oversee study plans; ensure compliance with GLP, SOPs, and quality standards. Monitor study progress, document deviations, coordinate with study personnel, and ensure accurate recording of raw data. Validate equipment and computerized systems used in studies. Maintain complete documentation of test systems and ensure proper archiving of all study records. Communicate effectively with Quality Assurance and provide required study documents. Conduct necropsy, tissue collection, organ weighing, processing, and staining when required. Prepare, update, and revise SOPs as needed. Subcontract work when required and document GLP compliance status. Perform any additional duties assigned by the HOD/TFM