78 Job openings found

Job title : Supervisor - GMP DocumentationDesired Qualifications : BSc./MSc./Diploma (Chemical)Experience Required : 1.0 Years+Industry : Pharmaceutical/ Fine/Speciality ChemicalsJob Function Dept- : Production (GMP)Location : DahejTechnical:? Having Batch processing experience on shop floor and familiar with equipment like reactor,centrifuge, dryer etc.? Having basic awareness about unit operation and unit process.? ...

Exp in Soft gelatine capsules manufacturing Knowledge of Gelatin Medicine Preparation Encapsulation Machine knowledge of documentation Of BMR and Log Book, SOP   Exp in Soft gelatine capsules manufacturing Knowledge of Gelatin Medicine Preparation Encapsulation Machine knowledge of documentation Of BMR and Log Book, SOP   Exp in Soft gelatine capsules manufacturing Knowledge of Gelatin Medicine Preparation Encapsulation Machine knowledge of documentation Of BMR and Log ...

ProductionReports To: Production Manager / Plant HeadLocation: Manufacturing PlantPurpose of the RoleTo schedule, operate, and monitor the production process of aroma chemicals(fragrance & flavour intermediates) in the plant, ensuring timely production in line withquality, safety, and output targets.Key Responsibilities1. Production Planning & Execution• Prepare and implement daily/ shift wise production ...

Department: Production Location: Manufacturing Plant Experience: 2–6 Years Qualification: B.Sc/M.Sc Chemistry or Diploma/B.E./B.Tech Chemical Engineering Key Responsibilities: Execute daily/shift-wise production plans and batch scheduling. Handle batch reactor, reaction, distillation, filtration, extraction & drying operations. Monitor process parameters such as temperature, pressure, pH and reaction time. Ensure compliance with SOPs, BMR, GMP/ISO and safety procedures. Coordinate with QC/QA, ...

Handling BMR- BPR Preparation Filling records as per cGMP RM - PM dispensing Validation Track & Trace Coordination with QA/QC Maintenance Dept, Maintain product quality and process safety Manpower Planning Perform other activities allocated by Production Head     Handling BMR- BPR Preparation Filling records as per cGMP RM - PM dispensing Validation Track & Trace Coordination with QA/QC Maintenance Dept, Maintain product quality and process safety Manpower ...

📌 Key Responsibilities Handle day-to-day API production operations as per BMR/BPR and SOPs. Operate and monitor reactors, centrifuges, dryers, filters and other process equipment. Execute batch manufacturing activities as per approved procedures. Monitor critical process parameters and ensure batch yield and quality. Maintain proper production documentation and ensure ALCOA+ compliance. Follow cGMP, SOP, EHS and safety ...

Machines / Equipment Candidates with hands-on experience in any of the following machines: Vial Filling & Sealing Machine Ampoule Filling & Sealing Machine Pre-filled Syringe Filling Machine Vial Washing Machine Key Responsibilities Operate aseptic area machines as per SOP, BMR and GMP requirements. Perform machine setup, operation, changeover and cleaning. Monitor machine parameters, filling accuracy, speed and output. Handle loading/unloading ...

Sr. No. Job Description1 Taking charge from previous shift by checking BMR and status of plant / batches foroperation in shift.2 To ensure that status of other activity is as per log report while taking charge fromoutgoing officer.3 During shift to ensure that GMP norms are strictly followed and to ...

🔹 Job Purpose To perform and monitor granulation activities in solid oral dosage (OSD) manufacturing while ensuring compliance with cGMP, safety, and quality standards. 🔹 Key Responsibilities ⚙️ Production / Operation Operate granulation equipment such as RMG, FBD/FBE, blender, etc. Execute wet / dry granulation processes as per BMR (Batch Manufacturing Record) Set machine parameters and ...

Key Responsibilities Production Documentation Prepare, review, and issue Batch Manufacturing Records (BMR) and Batch Production Records (BPR) Maintain daily production logs, shift reports, and production summaries Ensure timely and accurate documentation of production activities SOP & Record Management Draft, revise, and control Standard Operating Procedures (SOPs) related to production Maintain document control registers, master lists, and archival ...