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- ...compliance with cGMP, USFDA, and other regulatory requirements while meeting production targets. Key Responsibilities Supervise and execute production operations for granulation, compression, coating, and capsule filling. Ensure adherence to batch manufacturing records...Suggested
- ...and CAPAs related to production activities. Maintain compliance with USFDA, MHRA, and other global regulatory standards. Batch Execution & Monitoring Monitor batch manufacturing processes to ensure adherence to approved procedures. Coordinate with QA for line...Suggested
- ...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...SuggestedFor contractors
- ...Position: Engineering Executive Location: Amli Factory, Unilever Requisition ID : R-1171665 Job Summary The ASRS Engineering Executive... ...handling equipment. Strong understanding of PLC programming (e.g., Siemens, Allen-Bradley) and industrial control systems....SuggestedShift work
- ...Job Title Senior Officer / Executive – MSTG Orals Business Unit R&D1 Regulatory Affairs Job Grade G12A/G12B Location Dadra... ...Job Description To coordinate with different departments i.e. Formulation development (FDD), Analytical development (ADD), Packaging...Suggested
- ...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...SuggestedFull timeTraineeship
- ...per product development requirements. Perform innovator and market sample characterization for comparative evaluation. Plan and execute day-to-day F&D trials for Domestic, ROW, and other regulatory markets. Lead formulation development from pre-formulation studies...Suggested
- ...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...Suggested
- ...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. Guide and train operators and trainees on...SuggestedFull timeTraineeship
- Roles & Responsibilities: Ensure proper operation and cleaning of equipment and manufacturing areas related to Granulation, Compression, Coating, and Capsule Filling processes. Handle Change Control, Deviation, Incident, and Market Complaint activities in compliance with...Suggested
- 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...Suggested
- 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...SuggestedFull time
- ...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 meeting compliance requirementХ Tracking Approval rate...SuggestedFull time
- 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
- 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 ...Suggested
- 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
- ...Oral, and Ointment departments. Apply sound knowledge and experience in pharmaceutical formulations to ensure quality production. Execute granulation and compression processes efficiently and accurately. Maintain GMP compliance, personnel safety, and hygienic...Immediate start
- Role & Responsibilities: Prepare, review, and issue controlled copies of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Handle Change Control, Deviation, CAPA, and Investigation activities on the shop floor. Prepare and review Standard Operating...
- 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...
- 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...
