143 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 ...

Job Responsibilities:   Review & Control all QMS related document like change control, Deviation, out of Specification, CAPA and incident. Review of master BMR/BPR, SOP and specification. Preparation & review of departmental SOP. Participate in internal audit and coordinate for complies and closure. To coordinate in root cause and risk assessment. Review and maintain the executed documents ...

Key Responsibilities: Perform in-process checks during manufacturing and packaging (weight variation, hardness, friability, disintegration, pH, viscosity, leak test, etc.). Ensure batch manufacturing records (BMR/BPR) are correctly filled and compliant. Monitor line clearance, environmental conditions, and GMP practices on shop floor. Review and verify critical process parameters (CPP) and ensure adherence to SOPs. Check and approve ...

Duties & Responsibility :·       Quality Management System Implementation and Modification control.·       Document Control.·       Approval for batch release.·       Review and approval of Qualification Document.·       Review and approval of Calibration and Validation document.·       Planning, execution and compliance of both internal and external audits.·       Preparation of audit compliance report·       Review and approval ofSMF, VMP and Quality manual.·       Review and approval of BMR, ...

Major Responsibilities: Ø  Quality Management System Implementation and Modification control. Ø  Document Control. Ø  Approval for batch release. Ø  Review and approval of Qualification Document. Ø  Review and approval of Calibration and Validation document. Ø  Planning, execution and compliance of both internal and external audits. Ø  Preparation of audit compliance report.   Job description Minor Responsibilities:   Ø  Review and approval of SMF, VMP and Quality manual. Ø  Review and approval of ...

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 ...

Batch monitoring processing as per production plan Handling shift manpower e.g Operator, Helper Fill BMR Other documents as per ISO norms Batch monitoring processing as per production plan Handling shift manpower e.g Operator, Helper Fill BMR Other documents as per ISO norms Coordinate with maintenance department, QC department, RD Department Co Batch monitoring processing as per production plan Handling ...

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 ...

Production Executive Company: Concept Pharma Pvt. Ltd. Location: Aurangabad Vacancy: 1 Experience: 2–3 Years CTC (Budget): ₹Negotiable Key Responsibilities Oversee day-to-day production activities to ensure adherence to production plans, batch records, and schedules. Manage packaging operations to achieve quality standards and production targets while strictly following GMP norms. Coordinate with the Production Planning and Quality ...