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)
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, ...
5 Opening(s)
8.0 Year(s) To 12.0 Year(s)
4.20 LPA TO 5.00 LPA
Quality Control Chemist Job Description Template
Our company is looking for a Quality Control Chemist to join our team.
Responsibilities:
Perform analysis with a practical understanding of the test procedure and instrument operation;
Work under direction provided by supervisor and Other duties as assigned;
Maintain required level of training needed to perform a GMP task;
Organize ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.80 LPA TO 2.40 LPA
Job Summary: The Blister Operator is responsible for operating and maintaining blister packaging machines in a pharmaceutical manufacturing environment. This role ensures the efficient and accurate packaging of products in compliance with industry standards, regulatory requirements, and company policies.
Key Responsibilities:
Machine Operation:
Operate blister packaging machines to package pharmaceutical products according to ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.80 LPA TO 2.40 LPA
Job Summary: The SPM Operator is responsible for the operation and maintenance of Solid Preparation Machines (SPM) used in the production of pharmaceutical products. This role involves ensuring efficient and accurate processing, adhering to quality standards, and complying with regulatory requirements.
Key Responsibilities:
Operation of SPM Equipment:
Operate Solid Preparation Machines (SPM), including ...
6 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 10.00 LPA
Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...