Average salary: Rs750,000 /yearly

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  •  ...Officer / Executive – MSTG Orals Business Unit R&D1 Regulatory Affairs Job Grade G12A/G12B 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... 
    Suggested
    Diu
    3 days ago
  •  .... Manager – Global Quality Lead Business Unit Global Quality & Compliance Job Grade G9B Location : Mumbai 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 journey... 
    Suggested
    Contract work
    Diu
    3 days ago
  • 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...
    Suggested
    Una
    a month ago
  •  ...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... 
    Suggested
    Diu
    3 days ago
  • Job Purpose To oversee and manage day-to-day production activities in the Oral Solid Dosage (OSD) manufacturing area, ensuring compliance with cGMP, USFDA, and other regulatory requirements while meeting production targets. Key Responsibilities Supervise and execute...
    Suggested
    Diu
    3 days ago
  • Company Description Kaisha Lifesciences, a part of The Dadachanji Group of Companies, is an innovative pharmaceutical company dedicated to delivering safe, high-quality, and effective Injectable medications globally. The company focuses on enhancing the efficiency and ease...
    Suggested
    Full time
    Diu
    5 days ago
  • ORGANIZATIONAL STRUCTURE Job Title: Project Manager BUSINESS: INDIA-PUMPS LOCATION: DAMAN DIRECT REPORTING: Plant Head FUNCTIONAL REPORTING: Plant Head POSITION DETAILS The Project Manager has ultimate responsibility for the assigned project from the ...
    Suggested
    For subcontractor
    Diu
    3 days ago
  • Job Purpose To ensure compliance with cGMP, USFDA, and other regulatory requirements by implementing and maintaining Quality Management System (QMS) practices within the Production department. Responsible for documentation, deviation handling, and continuous improvement ...
    Suggested
    Diu
    3 days ago
  • Position: Electrical Executive Location: Amli Factory, Unilever Requistion ID:R-1171664 Job Summary The Electrical Executive will be responsible for the efficient operation, maintenance, and reliability of all electrical systems and equipment within our manufacturing...
    Suggested
    For contractors
    Diu
    2 days ago
  • 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) within...
    Suggested
    Shift work
    Diu
    2 days ago
  • Role & Responsibilities: Preparation of Analytical Method Validation (AMV) protocols, reports, and compilation of raw data. Execution of validation for compendial procedures as per USP General Chapter (1225). Performing validation of analytical procedures in accordance...
    Suggested
    Una
    a month ago
  • Job Title: Assistant Manager – ERP (Functional) ERP: Microsoft Dynamics 365 Business Central Function: ERP / Business Systems Industry: Manufacturing Reporting To: ERP Manager / Head – IT / Digital Transformation Job Purpose The ERP Functional Assistant ...
    Suggested
    Diu
    3 days ago
  •  ...Qualifications Qualification: Bachelor's degree in Chemical Engineering / M.Sc. Microbiology / M.Sc. Chemistry / M Pharm, preferably in the Pharma, FMCG or manufacturing sector. Experience: Minimum 2 – 3 Years in the relevant field/ Pharma / FMCG company. Key Skills Required... 
    Suggested
    Full time
    Diu
    2 days ago
  • Role description The role requires candidate serving as the subject matter expert in copper cable design, costing and application, and lead techno-commercial product solutions for the export market. RESPONSIBILITIES o Copper Cable Design o Provide technical and...
    Suggested
    Diu
    2 days ago
  • 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...
    Suggested
    Una
    a month ago
  • 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 ...
    Una
    a month ago
  • Job Overview 综述 The Production Scheduler is responsible for creating and maintaining a weekly production plan for the S&OE horizon. Scope of responsibility would be across multiple Celanese plants, yet within an individual region/ Business Line. They utilize scenario analysis...
    Diu
    6 days ago
  • Supervise and monitor vial ampoule and PFS packing lines as per BPR and SOPs. Ensure proper functioning of labeling sealing inspection and serialization machines . Review and maintain Batch Packing Records (BPRs) logbooks and line clearance documentation . Coordinate...
    Full time
    Traineeship

    USV

    Diu
    28 days ago
  • 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...
    Una
    a month ago
  • 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...
    Una
    a month ago
  •  ...ensure smooth manufacturing operations and compliance with regulatory requirements. Desired Candidate Profile: Qualification: B. Pharma Experience: 3 to 5 years of relevant experience in a similar role within a pharmaceutical formulation unit. Strong understanding... 
    Una
    a month ago
  • 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...
    Full time
    Traineeship

    USV

    Diu
    17 days ago
  • 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...
    Full time

    USV

    Diu
    a month ago
  • 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...
    Full time

    Bajaj Finance Limited

    Diu
    a month ago
  • 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...
    Work at office
    Una
    a month ago
  • Project Role : Business Analyst Project Role Description : Analyze an organization and design its processes and systems, assessing the business model and its integration with technology. Assess current state, identify customer requirements, and define the future state and...
    Full time
    Diu
    3 days ago
  • QMS Oversight: Manage deviations change controls CAPA and incident investigations related to OSD manufacturing operations. Root Cause Analysis: Conduct detailed investigations and impact assessments for deviations and process discrepancies. Documentation...
    Full time

    USV

    Diu
    more than 2 months ago
  •  ...Conduct cleaning validation sampling and documentation as per approved protocols. Required Candidate Profile: Qualification: B. Pharma / M. Pharma Experience: Minimum 1–2 years in pharmaceutical manufacturing (OSD preferred). Gender: Male candidates preferred.... 
    Una
    a month ago
  • Roles & Responsibilities: Responsible for manufacturing and monitoring batches in Tablet, Capsule, Liquid Oral, and Ointment departments. Apply sound knowledge and experience in pharmaceutical formulations to ensure quality production. Execute granulation and compression...
    Immediate start
    Una
    a month ago
  • Roles & Responsibilities: Perform analysis of Packing Materials (PM) and Raw Materials (RM) to ensure compliance with quality specifications. Prepare specifications for RM/PM and develop Standard Test Procedures (STPs) for testing. Carry out sampling of RM and PM as...
    Una
    a month ago