135 Job openings found

Job Title: Production Head - Pharma Pellet Manufacturing Facility Location: SB Organics, Chandapur Village, Hathnoora Mandal, Sangareddy District, Telangana Company Overview:SB Organics is a WHO-GMP accredited pharmaceutical pellet manufacturing facility dedicated to producinghigh-quality medicines. We are committed to adhering to the highest standards in manufacturing, ensuring the safety,efficacy, and compliance of our ...

Qualification: Graduate first Class and Material management diploma first class can be preferable.Relevant experience: min 12 to 20 Years Experience stores functioning from Chemical, Paint, Resins, Additives Industries.Work location: Nerul in Mumbai Job description:➢ Ensure availability of required raw materials by continuous follow up with Purchase as per production plan so ...

Key Responsibilities: 1. Production Planning & Execution Management: * Assist the Production Manager in developing and implementing daily, weekly, and monthly production schedules to meet demand forecasts. * Allocate resources (manpower, equipment) effectively to optimize production efficiency. * Oversee and monitor the execution of all production activities as per Batch Manufacturing ...

Aseptic Processing:  Overseeing and executing the manufacturing of APIs in a sterile environment, including compounding, filtration, and filling operations, while strictly adhering to aseptic techniques. cGMP Compliance:  Ensuring all production activities comply with current Good Manufacturing Practices (cGMP) and other relevant regulatory requirements (e.g., FDA, EMA). Documentation:  Accurate and timely completion and review of batch ...

Good Knowledge of USFDA/ EDQM /ANVISA / and all other regulatory & CGMP awareness. Strategic oversight and leadership: Develop and implement the company's quality management system (QMS) and strategy, aligning it with business objectives. This includes overseeing all aspects of quality operations and managing the QA and QC departments. Regulatory compliance: Ensure ...

Documentation & Compliance Prepare, review, control BMRs, SOPs, logbooks, and formats. Ensure cGMP & ALCOA+ compliance in documentation. Manage DocuSign workflows, approvals, revisions, and closures. Maintain archives for audits/inspections. Production Support Record and verify production data in SAP/digital systems. Coordinate with QA/QC/Engineering/Stores for timely closures. Review PISCADA reports with batch documentation. Support OQ/PQ documentation for equipment/utilities. QMS & Regulatory Manage QMS ...

Position:          Packing Incharge Location:         Mehsana Experience:     5 - 6 Years Industries:      Pharma    Responsibilities: Supervise and control online packing operations in accordance with EXCiPACT standards, cGMP and FDA guidelines and company procedures. Operate, monitor, and troubleshoot PLC, DCS, and SCADA systems to ensure smooth production processes. Manage packing team ...

Key Responsibilities: 1. Equipment & Facility Maintenance: Perform preventive, corrective, and predictive maintenance on manufacturing equipment and utilities. Maintain and update maintenance logs using CMMS (e.g., SAP PM, Maximo). Support qualification and validation activities (IQ/OQ/PQ) for equipment and systems. 2. Utility System Management: Operate and maintain utilities such as HVAC, AHUs, Boilers, Chillers, WFI, Purified Water ...

PRODUCTION EXECUTIVE Job Responsibilities• Responsible to maintain an optimum level of manpower and over time• Responsible to ensure all operation of production adherence to cGMP compliance• Responsible on manpower development (training) for quality, productivity and cost consciousness• To train the production personnel on cGMP Trend & regulatory requirement.• Monitor the work ...

Key Responsibilities: Documentation Management: Review, approve, and control various quality documents, including Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), Specifications, Test Procedures (STPs), and other quality-related documentation. Ensure proper archiving, retrieval, and revision control of all controlled documents. Participate in the preparation and review of site master files (SMF), ...