1 Opening(s)
3.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 9.00 LPA
Major Responsibilities:
• To ensure Proper Validation activity for new projects and changes in manufacturing in compliancewith The Company Policy and guidelines.• To ensure 100% validation documentation compliance as required by The Company Policy andguidelines.• Ensure periodic review of Validation documents.Identify the gaps in existing Validation documents and correction of the same.• Review the ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 6.00 LPA
Able to prepare PVP, URS, SIA, FMEA, JHA, FRS, DS, IQ, OQ, PQ protocols
Lead validation activities for projects, ensuring compliance with regulatory requirements and industry standards.
Execute validation protocols and procedures.
Conduct risk assessments and develop mitigation strategies.
Collaborate with cross-functional teams to ensure project objectives are met.
Review and approve validation documentation.
Provide technical ...
3 Opening(s)
1.5 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
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 ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Execute preventive and breakdown maintenance of all equipment's (Plant & Utility) as per respective equipment checklist and SOP.
Predictive Maintenance to Reduce Down Time
Ensuring that all activities are performed in accordance with cGMP, cGLP, Company SOP and health & safety policies at site.
Validation and Qualification of Equipment and Facilities.
Management of the ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 6.00 LPA
Execute preventive and breakdown maintenance of all equipment's (Plant & Utility) as per respective equipment checklist and SOP.
Predictive Maintenance to Reduce Down Time
Ensuring that all activities are performed in accordance with cGMP, cGLP, Company SOP and health & safety policies at site.
Validation and Qualification of Equipment and Facilities.
Management of the ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 7.50 LPA
Key Responsibilities:•Handling of QMS tools like change control, CAPA, Deviation etc.•Handle QA efficiently and able to maintain documentation as per GMP.•Preparation and maintenance of training schedule and co-ordinate with working staff to establish Procedures, Standards and System.•Preparation of Raw Material and Finished Product specification in accordance with Regulatory Guideline.•Vendor Evaluation, ...
1 Opening(s)
0.5 Year(s) To 2.0 Year(s)
1.44 LPA TO 2.50 LPA
Documentation & Compliance:
Maintain accurate and complete laboratory records in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
Prepare and review Certificates of Analysis (CoAs), test reports, and deviation reports.
Ensure compliance with company SOPs, safety protocols, and regulatory requirements (e.g., FDA, EPA, ISO).
Process Validation & Improvement:
Participate in validation of ...
3 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 4.50 LPA
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 & ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 8.00 LPA
Oversee day-to-day production activities for formulation batches as per approved BMR/BPR.
Ensure compliance with cGMP, GDP, and regulatory guidelines (WHO, EU, USFDA, MHRA as applicable).
Monitor production planning, batch scheduling, material requirement, and manpower allocation.
Coordinate with QA, QC, Warehouse, Engineering, and RA for smooth production operations.
Review and ensure timely completion of batch ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 3.60 LPA
We are looking for a Project Engineer with hands-on experience in installation, commissioning, and qualification of API equipment. The ideal candidate should have strong technical skills and prior exposure to API projects.
Roles & Responsibilities:
Handle installation and commissioning of API equipment.
Ensure equipment qualification as per regulatory standards.
Coordinate with vendors and contractors ...