Qa validation jobs in Diu

 ...reviews, instrument preventive maintenance/calibration/qualification/validation as per good manufacturing practices/good documentation...  ...review of all QC records related to Batch certification program. QA SME for manufacturing & packaging Investigations (Sterile & OSD)... 

 ...Investigate quality-related customer complaints and lead root cause analysis. Coordinate Corrective and Preventive Actions (CAPA) with Sales, QA, and Production teams. Documentation & Reporting: Maintain updated documentation for audits and customer reviews. Prepare and... 

 ...documentation for project orders # Transition from quality control to quality assurance # Support on-time delivery with timely completion of QA document packages, making of quality plan(QAP) for navy orders & review theQAP as per customer requirements for project/ETO orders and... 

 ...Packing Records (BPR), and relevant Standard Operating Procedures (SOPs). Participate in equipment and area qualification and ensure validation activities are conducted as per approved protocols and GMP standards. Support in maintaining documentation for validation,... 

 ...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 in... 

Company Description Udyogi is a leading safety solutions provider offering a wide range of integrated safety products, services, and training that adhere to global safety standards. With over 40 years of expertise, Udyogi specializes in risk assessment and the development...

Data and Documentation Review: Perform rigorous independent review of analytical raw data calculations instrument audit trails and final reports (including OOS and deviation investigations) to ensure compliance with quality standards (ALCOA). Compliance Oversight: Review...

 ...regulatory internal and customer audits ensuring adherence to CAPA closure timelines. Cross-functional Coordination: Collaborate with QA QC Engineering and Regulatory teams for implementation of QMS initiatives . Training & Awareness: Conduct training sessions... 

 ...Carry out equipment cleaning setup and changeover in line with SOP and validation. Document BMR entries logbooks and cleaning records as per GDP/GMP compliance . Coordinate with engineering/QA teams for troubleshooting and compliance checks. Follow strict... 

 ...expansions. Coordinate with cross-functional teams (Production, QA, QC, EHS) for smooth execution. Ensure timely completion of...  ...installation, and commissioning. Review technical specifications and validate vendor deliverables. Safety & Quality: Ensure adherence to... 

Company Description ESS ELL CABLES COMPANY is an copper and aluminium winding wire manufacturing company based in Daman,Daman & Diu, India. The company is known for producing high-quality enameled strip and round wire. ESS ELL CABLES COMPANY aims to ensure excellence...

 ...Maintain logbooks cleaning records and documentation as per GDP standards. Adhere to safety protocols gowning procedures and cleanroom discipline . Coordinate with QA and maintenance for smooth production and equipment upkeep. Required Experience: Junior IC... 

Company Description Treat Hotels & Resorts is dedicated to creating transformative, soul-enriching getaways that combine elevated design, warm hospitality, and immersive local flavors. Our destinations, spanning locations like Silvassa, Gholvad, Nashik, and Thane, offer...

 ...Role & 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... 

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...

 ...control systems. Manage electronic data backups and ensure data security and integrity. Provide IT support for computer system validation activities in QC and production environments. Act as a System Administrator, responsible for: User account creation and... 

 ...review Standard Operating Procedures (SOPs) and all formats related to manufacturing and packing operations. Prepare and control validation protocols and participate in process validation activities. Perform in-process monitoring during Dispensing, Granulation, Compression... 

 ...Description: Regulatory & Compliance Manager     1. Position Description   Job title Regulatory & Compliance Manager    Department QA Reports to Vice President-R&D Direct Reports - Location Daman       2. Job Purpose   Job Statement Job purpose Ensuring... 

Job Purpose This position is open with Bajaj Finance ltd. Duties and Responsibilities Х To achieve given Sales nos through customer walk in Х Work closely with the branch Service executives to drive Gold loan customers for fulfillment Х Ensuring policy adherence and...

Roles & Responsibilities: Operate and supervise packing operations and packing machinery efficiently. Ensure adherence to Good Manufacturing Practices (GMP) in all packing activities. Have knowledge of Packing Material (PM) dispensing activities and PM store...

Role & Responsibilities: Handle dispensing of Raw Materials (RM) and Packing Materials (PM) accurately as per batch requirements. Perform in-process quality checks to ensure compliance with defined standards. Review Batch Manufacturing Records (BMR), Batch Packing ...

Role & Responsibilities: Supervise Formulation & Development (F&D) activities and monitor operators/assistant operators within designated premises at the site. Conduct literature and patent searches and review findings as per product development requirements. Perform...

 ...serialization 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... 

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...

Role & Responsibilities: Receiving materials and preparing GRM (Goods Receipt Material) for Engineering, QC Chemicals, Raw Materials, and Finished Goods. Coordinating with the Purchase Head Office team regarding materials, documentation, and related queries. Handling...

 ...proper documentation of all testing activities, including test results, STPs, and specifications. Maintain GMP compliance in all laboratory operations and testing procedures. Coordinate with QA/QC and production departments for timely testing and release of materials.... 

 ...training to production personnel based on SOPs and maintain proper training records. Report all equipment breakdowns immediately to QA/Maintenance and track resolution until closure. Ensure preventive maintenance and calibration schedules are implemented, and equipment...