1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 6.00 LPA
To establish quality management system across all functions of plant related to quality
To execute & control QMS on a routine basis.
To prepare & approve all GMP related documents and control issuance, review, retrieval & storage securely.
To approve vendors for RM\PM.
To prepare specification, MOA, BMR, BPR, and control as per SOP ...
1 Opening(s)
15.0 Year(s) To 18.0 Year(s)
15.00 LPA TO 20.00 LPA
JOB DESCRIPTION:• P and ID’s preparation for Utilities (Clean & Black)• Should have experience in Basic & Detail Engineering for Mechanical, Piping, Instruments, pharmaceuticalWater System, Capacity analysis, Sizing and selection of equipment.• Project Planning and control, Project Procurement in Pharmaceutical domain• Preparation of load list.• Preparation of Equipment list for ...
10 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Documentation review and reconciliation. Responsible and ensuring following GMP.
Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements.
Team Leadership: Lead and supervise a team of granulation operators, ...
3 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.60 LPA
We are hiring a Production chemist, Production Officer in Palanpur.
Post: Production chemist, Production Officer
Location: Palanpur
Education: Bsc. in chemistry, Msc. in chemistry.Experience: minimum 1-5 year in API pharmaceutical industries’.Salary: Up to 30k CTC
Facilities: Canteen and also transport
Required skills: to be responsible for batch start up activity, monitoring, calibration of balance andother instruction ...
1 Opening(s)
8.0 Year(s) To 14.0 Year(s)
10.00 LPA TO 13.00 LPA
Over all the responsibilities of Quality Assurance.
Approval of documentation for all departments. Batch release of manufactured product.
Planning, execution and compliance of internal, external & International External Agencies audits.
Closure of all market complaints, product recalls or any other matter related to quality of products.
Implementation of GMP compliance in all the manufacturing ...
1 Opening(s)
4.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 6.00 LPA
Lead the development and implementation of quality assurance and control strategies to ensure product quality and compliance with standards.
Conduct and manage all quality audits, including internal, external, and supplier audits.
Analyse quality data to identify trends, root causes, and areas for improvement; develop and implement corrective and preventive actions.
Oversee and mentor ...
1 Opening(s)
0 To 3.0 Year(s)
1.80 LPA TO 2.50 LPA
Job Summary: We are seeking a highly skilled and experienced Quality Control Specialist with expertise in High-Performance Liquid Chromatography (HPLC) to join our pharmaceutical team. The ideal candidate will be responsible for ensuring the quality and safety of pharmaceutical products by conducting rigorous testing and analysis using HPLC and other ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Job Description:1. Awareness about GMP & practices2. Knowledge about Inventory Management , MIS, Stock Management & Manpower management.3. Knowledge of Store or Engineering Store management 4. Computer literacy for stock management
Job Description:1. Awareness about GMP & practices2. Knowledge about Inventory Management , MIS, Stock Management & Manpower management.3. Knowledge of ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.00 LPA TO 4.00 LPA
Responsible for analysis as per existing specification and test method.
Responsible for preparation of relevant documents like reports of analysis, certificate of analysis and approved/ rejected of the products.
Responsible for preparation of media /solutions of standards as per SOP.
Responsible for calibration, Qualification and validation of equipments/instruments and proper documentation.
Responsible for supervision ...
4 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Documentation review and reconciliation. Responsible and ensuring following GMP.
Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements.
Team Leadership: Lead and supervise a team of granulation operators, ...