187 Job openings found

Position :      Production Officer (Documentation) Location :      Vapi Experience:   2- 3 Years Industries:    Pharma - API Responsibilities: Coordinate with QA, QC, Purchase, and Warehouse for smooth production flow. Monitor raw material usage, yield efficiency, and finished product quality. Maintain cGMP compliance in all production operations and documentation.  Ensure shift-wise presence and manage production ...

🔧 Key Responsibilities Operate and monitor Blister Packing Machines (Alu-Alu / Alu-PVC). Perform machine setup, changeover, and format adjustments as per production plan. Ensure proper feeding of materials like PVC, Aluminum foil, and printed foils. Conduct in-process checks and maintain batch records as per SOP. Ensure compliance with cGMP, safety, and quality standards. Troubleshoot minor mechanical ...

Qualification & Experience M.Pharm / M.S / B.S in Chemistry, Pharmaceutics or related discipline 3–5 years of experience in R&D (DQA) Strong knowledge of GMP, GCP, GLP and 21 CFR 210/211 Experience with dermatology products or medical devices is an advantage Key Responsibilities Review development documents, analytical methods, R&D trials, lab notes, PDR, MFR, and batch ...

Position:          Shift Officer - Production (Pharma API) Location:         Vapi Experience:     2 - 3 Years Industries:      Pharma API Responsibilities: Execute API manufacturing activities as per Batch Manufacturing Records (BMR), SOPs, and GMP requirements. Operate and monitor reactors, centrifuges, filters, dryers, and other production equipment. Ensure accurate charging of raw materials and ...

The job description is as below: The R&D Manager - NDDS will lead formulation and development of novel drug delivery systems, from concept to scale up and tech transfer, ensuring compliance with regulatory and quality standards and alignment with business goals. The role requires strong scientific depth in NDDS, team leadership ...

Testing knowledge of all types of pigments testing. Having good knowledge testing of offset ink, liquid ink, UV ink and water base ink. Handling of instrument like X rite Spectrophotometer, TRM, UV Machine, IGT printer, KPP Automatic ink proofer & muller machine etc. Prepare test report and maintain excel sheet. Maintain all type of ...

Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable). Review and approve analytical results, COAs, test reports, and raw data. Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.). Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.). Review and update SOPs, STPs, GTPs, ...

Key Responsibilities: 1. Method Development & Validation Develop analytical methods for assay, dissolution, related substances, and stability testing. Conduct method validation as per ICH guidelines (accuracy, precision, specificity, linearity, robustness). Optimize and troubleshoot existing analytical methods. 2. Instrument Handling Operate analytical instruments such as HPLC, GC, UV, FTIR, KF, Dissolution Apparatus, etc. Perform daily calibration and ensure ...

  Process Excellence: Analyze and optimize manufacturing steps (e.g., granulation, blending, compression, coating, filling) to improve yield, throughput, and cycle time using continuous improvement methodologies. Troubleshooting & RCA: Quickly diagnose and resolve technical issues, equipment malfunctions, and production deviations, performing Root Cause Analysis (RCA) and implementing CAPAs (Corrective and Preventive Actions). Equipment & ...

  Perform scheduled Preventive Maintenance (PM) and rapid troubleshooting on AHUs, Chillers, Boilers, and associated mechanical and electrical controls. Maintain validated cleanroom conditions, including monitoring pressure cascades and supporting HEPA filter integrity checks. Document all maintenance activities accurately within the CMMS according to cGMP/SOP requirements. Assist in HVAC Qualification (IQ/OQ/PQ) activities. 2-6 years of HVAC ...