2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
REQUIREMENTS
Education / Experience
Education:
BSC / MSC Chemistry
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements
JOB PURPOSE
Generic
Implement Quality Assurance activities for Pharmaceutical at Dahej adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
🔹 Key Responsibilities
🖥 Control Room Monitoring
Monitor DCS graphics, process screens & trend logs
Control and maintain critical process parameters
Ensure smooth & optimal plant performance
âš™ Start-up / Shutdown Operations
Execute safe plant start-up & shutdown activities
Handle emergency procedures as per SOP
🔧 Troubleshooting & Deviation Handling
Identify process deviations
Diagnose issues and take corrective actions
Prevent equipment ...
1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 5.00 LPA
Manage the implementation of policies and maintain the discipline standards with the organization as desired / acceptable by the stakeholders.
Shall remain prepared for all possible emergency situations and responding to them as per the Emergency Management Plan.
Shall be responsible to maintain the high discipline standards within the team members as ...
15 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Looking for an experienced operator for batch process. Candidate must know how to handle chemicals and take reactions, monitor process, utility and prepare Batch Manufacturing Records.
Operate equipment
Monitor plant to ensure efficient production.
Must have experience of working in chemical industry
Loading / unloading / dispatch of RM tanker safely
Optimum utilization of resources ...
3 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 6.00 LPA
Job Responsibilities (Universal Chemicals)
Ensure all products meet quality standards and specifications.
Perform in-process and final product quality checks.
Review and maintain QA documents, records, and reports.
Prepare and update SOPs, specifications, and quality documents.
Monitor GMP, safety, and quality compliance in the plant.
Handle deviations, CAPA, and change control activities.
Participate in internal and external quality ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities
Perform analysis of raw materials, in-process samples, finished products, and stability samples.
Operate and maintain laboratory instruments such as HPLC, GC, UV, FTIR, and other analytical equipment.
Prepare, review, and maintain QC documentation, test reports, and laboratory records.
Follow Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and data integrity requirements.
Ensure compliance ...
1 Opening(s)
0 To 3.0 Year(s)
3.00 LPA TO 4.00 LPA
JD for Process Engineer: -Location: Jhagadia PlantDepartment: Process EngineeringExperience: 2-5 YearsQualification: B.E./B. Tech in Chemical Engineering.Budget: 7 LPA
Job SummaryWe are seeking a dynamic and result-oriented Process Chemical Engineer with 2-5 years of industrialexperience to support process optimization, scale-up activities, troubleshooting, and continuousimprovement initiatives. The candidate will work closely with Production, ...
3 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Key Responsibilities:
Perform analysis of Raw Materials (RM), In-Process Samples, Finished Products (FP), and Stability Samples.
Operate analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, and Dissolution Apparatus.
Prepare and standardize reagents, solutions, and reference standards.
Maintain analytical records, laboratory notebooks, and test reports as per cGMP and GLP requirements.
Perform calibration and routine ...
3 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 6.00 LPA
Job Responsibilities (Universal Chemicals)
Ensure all products meet quality standards and specifications.
Perform in-process and final product quality checks.
Review and maintain QA documents, records, and reports.
Prepare and update SOPs, specifications, and quality documents.
Monitor GMP, safety, and quality compliance in the plant.
Handle deviations, CAPA, and change control activities.
Participate in internal and external quality ...
3 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Key Responsibilities
Monitor and review calibration and preventive maintenance schedules, ensuring timely execution and accurate documentation.
Prepare, maintain, and update master lists, calibration records, and maintenance documentation while ensuring schedule compliance.
Manage instrumentation spare parts and material inventory, maintaining optimum stock levels for uninterrupted plant operations.
Coordinate Annual Maintenance Contract (AMC) activities, verify service ...