Executive export documentation jobs in Diu

 ...meeting production targets. Key Responsibilities Supervise and execute production operations for granulation, compression, coating,...  ...departments for smooth production flow. Ensure proper documentation and compliance with USFDA, MHRA, and other regulatory guidelines... 

 ...) practices within the Production department. Responsible for documentation, deviation handling, and continuous improvement initiatives to...  ...USFDA, MHRA, and other global regulatory standards. Batch Execution & Monitoring Monitor batch manufacturing processes to ensure... 

 ...machines . Review and maintain Batch Packing Records (BPRs) logbooks and line clearance documentation . Coordinate with QA Engineering and Warehouse teams for smooth batch execution. Ensure in-process quality checks and compliance with GMP and GDP practices.... 

 ...through customer walk in Х Work closely with the branch Service executives to drive Gold loan customers for fulfillment Х Ensuring policy...  ...for Gold loan product. Х Supporting Assayer in Operations /documentation. Required Qualifications and Experience Х Graduate with... 

 ...Job Title Senior Officer / Executive – MSTG Orals Business Unit R&D1 Regulatory Affairs Job Grade G12A/G12B Location...  ...process qualification batches To prepare and review new product documents like material requirement sheet, master formula card, bill of... 

 ...sample characterization for comparative evaluation. Plan and execute day-to-day F&D trials for Domestic, ROW, and other regulatory...  ...evaluation of developed formulations. Prepare and review technical documentation, including Product Development Reports (PDRs), Master Formula... 

 ...Group, we aim to redefine the essence of staying and traveling. Role Description This is a full-time, on-site role for an L&D Executive located in Silvassa. The L&D Executive will be responsible for planning and facilitating training sessions, managing learning... 

 ...Responsibilities: Perform Analytical Method Validation (AMV) activities, including designing validation protocols, executing validation studies, and documenting results for analytical methods used in raw materials, in-process, and finished product testing. Participate in... 

 ...management. Perform reconciliation of packing materials to ensure accuracy and avoid discrepancies. Maintain all packing-related documents as per cGMP requirements . Ensure compliance with company policies and quality standards during packing operations.... 

 ...proper handling and storage of control and stability samples as per SOPs. Maintain compliance with cGMP during all in-process and documentation activities. Preferred Candidate Profile: Experience in an OSD (Oral Solid Dosage) plant. Familiarity with in-process... 

 ...Role & Responsibilities: Manage and maintain all documentation related to Quality Management Systems (QMS), including validation, qualification, deviation, and change control activities. Prepare and review MFRs, SOPs, and AMV (Analytical Method Validation) documents... 

 ...procedures and regulatory guidelines. Maintain sound knowledge and implementation of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) across manufacturing activities. Prepare and review Batch Manufacturing Records (BMR), Batch Packing Records (... 

Routine & Non-Routine Analysis: Perform complex testing on raw materials packaging and finished products using advanced instrumentation (e.g. HPLC GC UV-Spectroscopy). Stability Testing: Monitor product samples over time to ensure they maintain quality under various environmental...

 ...Job Title Executive / Sr Officer Business Unit Administration Job Grade G12 A / G12 B Location : Dadra At Sun Pharma, we commit to helping you 'Create your own sunshine' — by fostering an environment where you grow at every step, take charge of your... 

 ...Position: Engineering Executive Location: Amli Factory, Unilever Requisition ID : R-1171665 Job Summary The ASRS Engineering Executive will be responsible for the maintenance, troubleshooting, and optimization of Automated Storage and Retrieval Systems (ASRS)... 

 ...Engineering, QC Chemicals, Raw Materials, and Finished Goods. Coordinating with the Purchase Head Office team regarding materials, documentation, and related queries. Handling damaged, expired, or obsolete Engineering, Consumable, Miscellaneous, and QC Chemical items as... 

The QC Micro Environmental Monitoring Officer will be responsible for performing environmental monitoring and microbiological testing to ensure that all production and laboratory areas comply with GMP and regulatory standards. This role ensures the safety and quality of pharmaceutical...

 ...analytical instruments and laboratory equipment, ensuring accurate results and compliance with calibration schedules. Ensure proper documentation of all testing activities, including test results, STPs, and specifications. Maintain GMP compliance in all laboratory... 

 ...performed during manufacturing and that results meet quality standards. Review BMRs, logbooks, in-process formats, and other online documentation for accuracy and completeness. Conduct cleaning validation sampling and documentation as per approved protocols. Required... 

 ...in pharmaceutical formulations to ensure quality production. Execute granulation and compression processes efficiently and accurately...  ...practices on the shop floor. Ensure online completion of production documents such as BMRs and BPRs. Provide periodic training to... 

Role & Responsibilities: Monitor the Server Room to ensure the proper functioning of systems, servers, and network operations. Manage time synchronization of production and Quality Control (QC) equipment. Perform maintenance and troubleshooting of IT hardware and software...

 ...Job Title Executive / Sr Officer Business Unit Administration Job Grade G12 A / G12 B Location : Dadra At Sun Pharma, we commit to helping you 'Create your own sunshine' — by fostering an environment where you grow at every step, take charge of your...