876 Executive Jobs - Page 15

Job Title: Material Expeditor Position Summary The Material Expeditor is responsible for ensuring the timely delivery of materials, components, and equipment from suppliers to support ongoing operations and projects. Based at the Head Office, this role involves close coordination with suppliers, internal teams, and logistics providers to track orders, resolve delays, and maintain accurate delivery schedules. Key Responsibilities Order Follow-up & Tracking Monitor purchase orders to ensure timely delivery of goods. Maintain updated records of order status, shipment schedules, and delivery dates. Follow up with suppliers regularly to confirm manufacturing and dispatch timelines. Supplier Coord...

Company Description Paramount Health Services & Insurance TPA Pvt. Ltd. (PHS) is a leading Third Party Administrator (TPA) in the Health Insurance sector, servicing all insurance companies. PHS enhances health insurance policies for individuals by adding value through a network of healthcare service providers, medical care standardization, claims management, client servicing, and expert opinion. PHS customizes healthcare delivery to administer comprehensive healthcare packages for its clients. Role Description This is a full-time on-site role for an Executive, located in Mumbai. The Executive will be responsible for day-to-day operations including client servicing, claims management, coordin...

Executive with good communication, smart looking and willing to work in target based team

The Executive position at Buffcon, located in Bihar, is a full-time on-site role where you will be responsible for overseeing daily operations, managing staff, and ensuring adherence to company policies and procedures. Your role will involve developing and implementing strategies for business growth, managing budgets, and engaging with stakeholders. Furthermore, you will analyze performance metrics to identify areas for improvement and uphold customer satisfaction. To excel in this role, you should possess leadership, management, and supervisory skills. Your strategic planning and business development capabilities will be crucial, along with financial management and budgeting proficiency. Ef...

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...

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...

" Responsible For rDNA manufacturing and Parenteral mfg activities at Dholka premises To ensure personal hygiene of the workmen before entering to aseptic area and maintain record. To check and ensure that aseptic area workmen are following entry exist procedure properly. To check and ensure that differential pressure, RH and temperature of the aseptic area and mfg area are within limit and record it properly. To check and ensure that differential pressure of all Laminar Air Flow are within limit and record it properly. To check on line in process parameters like temperature, RH, fill volume, quality of sealing at specific interval as mentioned in respective MMDI and SOPs and record the same...

Execution of plans for cell culture group Preparation of media for cell culture purpose Preparation of buffers Cell Line maintenance Calibration of pH meter Handling and knowledge of Bioreactor (STR and Wave) Cell propagation for different projects Performing Cell Count and metabolite analysis. Compiling of data, forms and report preparation Aseptic handling and sterile Area Maintenance Maintaining inventory of cell culture related products SOP preparation and periodic revision

" Responsible for compression activity in Penicillin department. To enforce CGMP compliances in the department. To maintain higher standard of quality during compression. To coordinate interdepartmental and resolve the issues pertaining to product. To improve the productivity. Production planning so as to meet the effective implementation of Plan To discuss and give feedback on day to day production planning for any shortage to department. To review daily production and to discuss other issues. To complete BMR of daily production & transfer finished goods on daily basis. To coordinate with Eng. Department for preventive maintenance of various machine also Report and follow up on breakdown ma...

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...

Major Purpose of the Job: Development of purification process for recombinant proteins. Principal Tasks and Responsibilities: Stock buffers and working buffer preparation pH and conductivity meter operation Column packing for purification Column cleaning (Pre and post run CIP), maintenance and storage Independently handle protein purification system example AKTA purification system Protein concentration using TFF, and different concentration system Documentation and preparing presentations of data generated. Ensuring good laboratory practices in DSP In the absence of the job holder the designee assigned by the reporting manager would be responsible for carrying out the above responsibilities...

" Compliance to cGMP and other regulatory requirement. To monitor the daily packing activates in primary packing in with compliance of cGMP norms. To execute packing inputs as per shift plan in Advanced & achieve it. Ensure compliance of the online Documents during packaging process. To ensure the packing activity as per Respective SOP. To Monitor & Minimize the process loss during packing operation. Perform the In process checks for the Correctness of the packed Product. Stage wise Reconciliation of the Product/Packing material. Coordination with the Different Supportive department for the fulfilment of the Department requirement."

To perform the technology receiving activities and QMS related activities at the manufacturing plant. To perform technology-receiving activities by receiving processes from upstream process development to manufacturing and/or between multiple manufacturing sites. This includes developing and maintaining key SOPs, manufacturing records to support compliance with quality management and regulatory submissions. To perform alternate vendor batch execution, process improvement, change in batch size, trouble shooting at shop floor, equipment change activities of product after technology transfer completion along with production team. To coordinate the development of the manufacturing process with t...

" Responsible for small volume parenteral manufacturing activities at Dholka premises. To check hygienic condition of the workmen before entering to aseptic area, processing area and compounding area and maintain record. To check and ensure entry exist procedure of workmen with proper gowning and sanitization. To check and ensure that Temperature and differential pressure of the all area is within limit and record it properly. To check on line in process parameters like temperature, RH, fill volume, quality of sealing at specific interval as mentioned in respective MMD-I and SOPs and record the same in BMR To check and ensure that sterilization of the containers, equipment's, utensils etc. a...

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...

Follow cGMP and GLP PRACTICES. To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed / implemented properly. To follow safety Procedure in QC department. To manage an accurate, reliable, efficient and timely review of finished products, in process/ validation, raw material, stability, GLP, Non-routine samples. To ensure timely review of batch audit trail, system audit trail, message center. To ensure review of Logbooks of instrument, equipment’s, columns, standards, impurities etc. To review the COA of finished product in LIMS after the completion of analysis. To ensure the status label updated for the instruments, ...

1 Ensure Freedom to operate of CPL's product (Formulation) 2 Design a strategy to secure CPL's invention effectively 3 Handling of Patent Prosecution 4 Effective Management of CPL Patent Portfolio 5 Support to New Product Selection Activity

Major Purpose Of The Job To developed Analytical Method Development, Routine analysis and Validation by GC & GC-MS To maintain and observe cGLP and cGDP in working environment in GC & GC-MS. Timely respond development of the Regulatory Queries of products. Preparation of COA’s. Follow and update periodic Preventive Maintenance & Calibration schedule of GC & GC-MS DSC; TGA instrument. Responsibilities Preparation of NewAnalytical method validation and Method Transfer Protocol and Report as per the current Regulatory requirement. Prepare Protocol of analytical method validation and method transfer report and routine analysis data. Preparation of standard operating procedure. Maintaining GC & G...

Major Purpose: (Exactly spell out key deliveries/results expected from this job) Preparation of New product Specifications and Standard test procedures for ANDA, Export and Domestic markets. Preparation of Routine revision Specifications and Standard test procedures for ANDA, Export and Domestic markets Responsibilities: (Please write all the major jobs that the employee is required to carry out ) Preparation of New product documents and Routine Revision of Raw Material Specifications and Standard Test Procedures for Export, Regulatory agency and Domestic market. Preparation of New product documents and Routine Revision of Finished Product Specifications and Standard Test Procedures for Expo...

Ensure Freedom to operate of CPL's product (Formulation) Design a strategy to secure CPL's invention effectively Handling of Patent Prosecution Effective Management of CPL Patent Portfolio Support to New Product Selection Activity

This role would be part of Analytical Research & Development for Formulations Research team. The key responsbilities would be as mentioned below: Analytical methods validation and report preparation on LCMS (for Nitrosamine impurities, NDSRI impurities etc.) Analytical Method development and report preparation on LCMS (for Nitrosamine impurities, NDSRI impurities etc.) Routine and stability sample analysis Analytical method verification of drug products and drug substances on LCMS Key Skills Required Analytical method development by LCMS & validation Trouble shooting of Instruments Impurity maintenance

" 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...

Ensure efficient operation and maintenance of Utility (Boiler, chilling plant, Air compressor, cooling tower and N2 System). To ensure strict compliance of cGMP requirements & Good Engineering Practice requirements besides other statutory laws, rules and regulations. To implement Cost reduction measures in the operation of the Utility. To prepare and maintain SOP and documents related to machine operation and maintenance. To identify probable cause/potential non-conformity to any breakdown/abnormal condition. To perform breakdown maintenance activity as and when applicable. Review machine operation related documents and equipment log books. To prepare schedule for planned activities like pre...

Method verification of new HPLC method for all stages of new molecule as well as modified old molecule method as per regulatory guidelines. Calibration and maintenance of HPLC systems as per SOP. Maintaining records for all analytical reports by entering all the data in raw note book and timely release of analytical report. To maintain analytical data and report.

"1. Planning and execution of Validation, Qualification, Re-Qualification and Re-Validation activities pertaining to Manufacturing facility at Dholka site in line with the cGMP requirements of national and international regulatory authorities. To Perform Vendor Management Activity to assure that Vendors are Complying with Cadila SOP on Vendor Management and GMP Requirements in Order to source Quality Materials and Products. To perform the validation exercises of new as well as existing equipment’s, utilities and critical systems. Preparation, Execution, Compilation & Review of qualification and Validation Protocols & Reports. Preparation of SOPs pertaining to qualification and Validation act...