876 Executive Jobs - Page 16

Compilation, review and submission of registration dossiers in the regions of South East Asia Handling of regulatory queries/deficiencies across all the South East Asia countries Submission of Supplements/Variations across all the South East Asia countries Review of functional documents such as Specifications/Test Procedures/Product Development Reports/Stability Protocols etc. and Review and approval of Change Controls & Deviations Ensure availability of current guidelines for South East Asia Establish co-ordination with other departments like QA/QC, R&D, Marketing and Purchase for ensuring the filings and query response within period Submission of various original documents for notarization...

Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. Logistics & Distribution Ensure timely dispatch of f...

Data Collection & Management Collect, organize, and maintain data from various internal sources (e.g., financial, operational, sales, and customer data). Ensure the accuracy and consistency of data by verifying and cleaning the data sets. Support data entry, database maintenance, and ensure data is stored and updated correctly in the system. Reporting & Dashboards Prepare and generate daily, weekly, and monthly reports on key business metrics, with a focus on Sales Force Effectiveness (e.g., sales productivity, sales cycle, conversion rates, etc.). Create and maintain dashboards to track the performance of the sales team, identifying key performance indicators (KPIs) related to sales product...

Follow cGMP and GLP practices in Quality Control Lab. To analyze the Sample of stability on instrument such HPLC, UV, FTIR etc. by following test procedure. Analysis of Stability Samples as per schedule To follow safety procedure in QC department. To attend the training as per schedule. To receive the samples for analysis and making entry in Inward register. To maintain the Instruments log books related to sample analysis. To analyze the sample and compilation of documents. Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS. Responsible for online documentation. To do any other Work assign by HOD.

Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. Logistics & Distribution Ensure timely dispatch of f...

"1) Based on production requirement generate the production plan for next 3 month. Run MRP for next 3 month in System (SAP) Share the shortages to RM / PM based on requirement to Purchase team. Discuss and coordinate with purchase team for timely supply RM / PM Discuss with Production team for scheduling of products. Delivery has to completed for M0 for ISBU / USBU on 22nd and for BSBU on 25th Prepare the plan Vs Actual on daily basis. Generate the LL requirement separately after discussion with LL team. Closely coordinate with cross function department for Ach goal. Daily discuss with Production / QC and purchase team for ach daily schedule. To provide technical support for change managemen...

Preparation of CTD/eCTD format drug master file and its submission to various regulatory authorities including USA, Europe, Canada, Australia, China, Japan, Korea, Brazil and ROW market Preparation of query response of drug substance for various and less regulated markets and customers. Preparation of applicant part and closed part for various authorities for different customers. Preparation of annual updates and amendment of drug master files US via ESG, ASMF via CESP, KDMF via MFDS Korea, Preparation and submission of CEP applications and responses to EDQM via CESP. Preparation of CEP LOA’s & LOA’s and declarations of various customers and authority. To collect and evaluate scientific data...

" Follow cGMP and GLP practices in Quality Control Lab. To analyze the Sample of stability on instrument such HPLC, UV, FTIR etc. by following test procedure. Analysis of Stability Samples as per schedule To follow safety procedure in QC department. To attend the training as per schedule. To receive the samples for analysis and making entry in Inward register. To maintain the Instruments log books related to sample analysis. To analyze the sample and compilation of documents. Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS. Responsible for online documentation. To do any other Work assign by HOD."

Major Purpose Of The Job Negotiation with vendor for lowest price. New vendor development for alternate source. SAP operation. Market information. Resolving day to day issues with internal and external customers. Team work. Cross functional meeting with internal customers for update and issue resolution. Follow up with vendors for delivery / quotation and if any requirement for our internal customers Ensure timely delivery of primary & secondary packaging materials for each location Ensure timely vendor payments Principal Tasks And Responsibilities Negotiation Ensure Quotations from different vendors are arranged as per SOP Verification of Comparative Analysis and negotiation Finalize the pr...

" Follow cGMP and GLP practices in Quality Control Lab. To analyze the Sample of stability on non-chromatographic instrument such as FTIR, UV, Dissolution, DT, Hardness etc by following test procedure. Analysis of Stability Samples as per schedule To attend the training as per schedule. To follow safety procedure in QC department. To receive the samples for analysis and making entry in Inward register. To maintain the Instruments log books related to sample analysis. To analyze the sample and compilation of documents. Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS. Responsible for cleaning & monitoring of laboratory. Responsible for onl...

Working on Unit operations related to downstream processing during Drug Substance (DS) manufacturing. GMP documentation related to DS manufacturing like batch records, equipment usage, facility monitoring. Preparation of documents like SOPs, MMDS and QMS related documents like change control, deviation, CAPA, risk assessment etc. Monitoring of manufacturing facility and keep it cGMP compliant Involvement during regulatory audit preparation Co-ordination with cross functional teams like QC, QA, Maintenance, Warehouse, Injection etc. Training and mentoring new joinees Keep the track for calibration and qualification activities, for example for equipment, weighing scale and standards etc

To prepare and maintain SOP and documents related to Plant preventive maintenance. To conduct routine breakdown maintenance of Main Pharma Block equipment’s. To follow and implement PPM schedule for effective implementation in shortest duration of time for all equipment’s in close co-ordination with production dept. To allocate maintenance job to all the technicians with routine breakdown requisition. To co-ordinate with inter department staff for any breakdown or any abnormality in equipment’s. To provide support to Execution of CAPEX project of process equipment side. Ensure timely indenting of spares required for preventive maintenance / breakdown maintenance with close follow up with sen...

Greetings and welcome visitors Manage Front Desk Handle phone calls Manage conference rooms Maintain Records Perform administrative task

Production Supervision of production & maintenance activities of respective shift. To ensure that every raw material used is of right quality (approved from QC, having reference Number) and quantity (verifying the weights, if required by re weighing) in every batch Automation/DCS knowledge required to run the plant in all 3 shifts. To ensure all liquid charging through automation/DCS system. To ensure all solid charging through PTS (Powder Transfer System). To ensure all monitoring through DCS system. To ensure 100% implementation of process conditions for batch as per BPRs. To take instruction from managers for batch charging / monitoring & to execute. To ensure maximum utilization of plant...

Procurement Coordination Raise and process purchase orders for raw materials, packaging materials, and other items as per requirements. Follow up with suppliers for on-time delivery and resolve any supply-related issues. Coordinate with QA, QC, and stores for GRN and material clearance. Inventory Management Monitor and maintain optimal inventory levels for RM/PM/FSM (Raw/Packaging/Finished Stock Material). Reconcile stock regularly with warehouse and update ERP records. Work with production planning to avoid stock-outs or excess inventory. Logistics & Dispatch Coordinate with transporters for dispatch planning and delivery of finished goods to customers/C&F. Track shipments and resolve logis...

To supervised all activity of shop floor of production department. To handle the men power as per shift. To handle the shift as per production planning. To handle the dispensing activities. To supervised the manufacturing area, autoclave area, vial washing and depyrogenation tunnel and filling related activities. To handle the troubleshooting of production area with the help of supporting department. To ensure calibration certificates of all measuring instruments comply with norms. To check hygienic condition of the workmen before entering to aseptic area and maintain record. To check and ensure that aseptic area workmen are following entry exit procedure properly. To check and ensure that p...

Supervision of production & maintenance activities of respective shift. To ensure that every raw material used is of right quality (approved from QC, having reference Number) and quantity (verifying the weights, if required by re weighing) in every batch. To ensure 100% implementation of process conditions for batch as per BPRs. To take instruction from managers for batch charging / monitoring & to execute. To ensure maximum utilization of plant equipment & manpower in respective shift. To report any deviation / discrepancy in plant / process to his to reporting manager. To ensure completion of batches as per plan. To do SAP transaction related to production module. Documentation : To ensure...

Documentation To prepare SOP’s/ URS/ BPR/ Protocol/ Investigation report for regulatory compliance as per available procedure/practice. Ensure that all documents / records required for Regulatory Compliance are maintained properly. Ensure old records are archived properly and are retrievable. To check online filling of document & online submission to QA department. Raise change control/ Deviation/ CAPA in OASIS LIMS. To support SAP transaction in production module as & when required. Raise indents for Consumables, parts, Stationary and Spares required for the plant. To ensure for high standards of housekeeping in plants. To maintain all records and documents as per GDP/SOPs. To take lead in ...

To maintain and adherence of the GLP and safety procedures in laboratory. To raise the request for issuance of work data sheet / protocols. To perform the analysis as per work allocation and records the results in work sheet / protocol and maintain on line documentation. To maintain the CFR 21 part -11 compliance by following laid down procedures. To perform all the HPLC related analysis of In-process, finished products & returned goods / Hold time / Stability study /reference / working standard analysis as per laid down specification & test procedures , SOPs, as per work allocation and report the analysis data in LIMS modules and report to Section – Head. To ensure that every specification ...

Operate Effluent Treatment Plant., MEE, and RO in the shift and maintain all the parameter. Ensure the functioning of Effluent Treatment Plant MEE and RO in good condition. Ensure proper maintenance of all equipments in the working area. Liaise with local agencies like AEPS, NCTL, etc. Ensure proper disposal of ETP Sludge to BEIL site. Analysis to be done and record keeping of Effluent Treatment Plant. Maintain all documents in the department. Take plant round and check effluent discharge and housekeeping. Report any abnormalities found to dept. head. Collect data of hazardous waste generation and general scrap waste and maintain records. Ensure proper disposal of effluent after checking the...

To maintain and adherence of the GLP and safety procedures in laboratory. To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermediates /APIs/ Stability and etc.. as per current specification and method of analysis. To work as Analyst and maintain the CFR 21 part -11 compliance by following laid down procedures. To perform all the HPLC related analysis and perform the online documentation for In-process, intermediate, finished products & returned goods / raw materials Hold time / Stability study / working standard analysis as per laid down specification & test procedures , SOPs, as per work allocation and r...

Ensuring seamless Induction as per SOP & Corporate Guidelines. Evaluate and improve Induction process time to time Ensure Employee Engagement Initiatives driven in that plant in a planned and effective manners Ensure all QMS related activities are closed as per timeline Prepare and Maintain NEOP (New employee orientation Programme) as per SOP. Prepare Monthly Training Calendar and ensuring effective implementation as per Requirement. Ensure to monitor training effectiveness Preparation of Individual Training File and creating awareness and ensuring its implementation. Maintain JD for all the available roles in the plan and review at regular intervals Regularizing employees attendance to ensu...

Documentation To prepare SOP’s/ URS/ BPR/ Protocol/ Investigation report for regulatory compliance as per available procedure/practice. Ensure that all documents / records required for Regulatory Compliance are maintained properly. Ensure old records are archived properly and are retrievable. To check online filling of document & online submission to QA department. Raise change control/ Deviation/ CAPA in OASIS LIMS. To support SAP transaction in production module as & when required. Raise indents for Consumables, parts, Stationary and Spares required for the plant. To ensure for high standards of housekeeping in plants. To maintain all records and documents as per GDP/SOPs. To take lead in ...

We are hiring Executive profile for Health Insurance TPA Co. Job location will be Goa. Minimum 1-3 year experience of health Insurance Healthcare Industry and PIMS exp. will be preferred. Freshers can also apply. Job Types: Full-time, Permanent Benefits: Health insurance Provident Fund Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Health insurance Work Location: In person

Skills: Basic MS Office knowledge, good communication skills, coordination ability. Responsibilities: Handling day-to-day admin activities, maintaining records, coordinating with vendors, and supporting office operations.