Core Responsibilities: Bookkeeping & Record Maintenance Maintain day-to-day financial records and ledgers. Ensure accurate and up-to-date entries in accounting software (e.g., Tally, SAP, QuickBooks). Accounts Payable and Receivable Process vendor invoices, payments, and staff reimbursements. Follow up on customer payments and manage receivables. Reconcile statements with vendors and customers. Bank Reconciliation Regularly reconcile bank statements with company accounts. Report any discrepancies or irregularities. GST & Tax Compliance Assist in preparing and filing GST returns. Support TDS calculations and timely filing. Maintain compliance with local tax regulations. Financial Reporting Prepare basic financial reports such as profit & loss statements, balance sheets, and cash flow statements. Assist in preparing monthly, quarterly, and annual financial reports. Audit Support Assist internal and external auditors during audits. Compile necessary documentation and support schedules.

Role & responsibilities: 1. Should have hands-on experience in manufacturing of plasma derived proteins like IgG, Albumin, clotting factors etc. 2. Hands on experience in nanofiltration of plasma derived proteins. 3. Experience in URS preparation and qualification of equipments in downstream manufacturing facility. 4. Should have experience in handling chromatography systems like AKTA process, AKTA Pilot etc. and execute chromatography operations. 5. Should have experience in handling different columns like BPG column, chromaflow column and Axichrom column including its packing and unpacking. 6. Should have experience in handling continuous centrifuge. 7. Should have experience handling Semi-automatic and manual TFF systems . 8. Execute and monitor supporting activities like steam sterilizer, DHS, Filter integrity machine etc. 9. Should have experience in handling stainless steel vessels, single use bags and CIP/SIP skids . 10. Experience in preparing the solution/buffers for downstream operation. 11. Experience in execution and review of batch manufacturing records, solution preparation records, log books etc. 12. Experience in keeping the facility neat and clean with respect to internal and external audits. Initiation of QMS documents like Change control, Deviation, Risk assessment, CAPA, change implementation and effectiveness verification and support for closing open documents on time. Qualification: M.Sc/M.Tech/B.Tech