50 Job openings found

🔹 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: Execute day-to-day operations in aseptic and sterile manufacturing areas Monitor LVP production activities in compliance with SOPs, cGMP, and regulatory guidelines Operate and maintain critical equipment including autoclaves, filling machines, and sterilizers Ensure strict adherence to safety, quality, and environmental standards Prepare, review, and maintain batch production records and related documentation 🔹 Qualifications ...

Job Title: Design Engineer (Mechanical) Location: Ahmedabad Experience: 2–5 Years Qualification: B.E. Mechanical Salary: ₹4.5 LPA Job Summary: We are looking for a skilled Design Engineer with hands-on experience in mechanical product design, particularly in plastic auxiliary equipment and thermal systems. The candidate should be proficient in 3D CAD tools, engineering documentation, and ...

Job Title: Backend Java Developer Location: Reading, PA (onsite 2 days/week)- locals only  Client: Penske Truck Visa: USC / GC / H4 EAD Exp level: 15+ years  F2F Interview required (1 round process – 2 hour in person interview w/ coding) Job Description: Act as the primary support contact for multiple applications, handling the complete application lifecycle: ...

• Ensure cGMP, Good Documentation Practices (GDP), Data Integrity, and Data Security Policies are followed. • Oversee and validate various software in quality control and assurance functions, such as HPLC, IR, UV, and Stability Control systems. • Manage user accounts, roles, and access rights for quality systems and instruments. • Backup/archive QC data ...

Analysis of Inprocess, Intermediate, Raw Material, Stability and Finished product samples as per approved specification/Test method/Protocol and recording of analytical data in to analytical data sheet.   Prepare and standardize the volumetric solution and reagent as per SOP  by following the Good Laboratory practices, Good documentation practices during the analysis.   To prepare QC ...

To follow good documentation practices & good laboratory practices & encourage subordinate to maintain the same. To ensure execution of safety precautions in the laboratory. To perform daily operation & calibration of pH meter & balance. To maintain hplc & gc column & hplc & gc instrument. To record daily temperature monitoring of analytical ...

Lead Production-related QMS activities including SOPs, Deviations, CAPA, Change Control, and Risk Management. Lead OOS/OOT investigations with QA/QC and provide technical inputs. Review batch records, process parameters, equipment, materials, and manufacturing history. Drive root cause analysis, impact assessment, and scientifically justified conclusions. Lead investigations for deviations, process failures, batch discrepancies, yield variations, and equipment ...

Position:      Shift Incharge - Production Location:       Vapi Experience:  4 - 8 Years Industries:    Chemical  Responsibilities: Handle complete plant and shift operations safely and efficiently Supervise and manage shift manpower Ensure smooth execution of production activities as per plan Troubleshoot process, equipment, and operational issues Investigate root causes for failures, deviations, and abnormalities and implement ...

YOUR TASKS Good understanding of automotive communication protocols such as CAN, LIN, SPI, I2C, and UART. Good understanding of thermal management techniques for LED lighting and electronics applications. Familiarity with PLM tools, change management processes, and engineering documentation practices. Ability to review schematic designs, PCB layouts, and manufacturing documentation. Understanding of analog and digital hardware ...