1 Opening(s)
0 To 3.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: Production Chemist/Officer/Executive
Location: Vapi
Experience: 0 - 3 Years
Industries: Pharma API
Responsibilities:
Handling API production activities as per BMR/BPR
Monitoring process parameters and maintaining batch records
Ensuring compliance with GMP and safety norms
Coordination with QA/QC and Engineering departments
Maintaining proper documentation as per regulatory requirements
Requirements :
Logical thinking.
Organizing.
Good in communication.
Basic ...
10 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Experience in API / Intermediates manufacturing company2. Working as per SOP and follow the safety protocols3. Working experience in GMP environment4. Maintaining Documentation / BMRGood Manufacturing Practices (GMP) are a system ensuring products like food, drugs, and cosmetics are consistently made and controlled to quality standards, minimizing risks like contamination and ...
10 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Experience in API / Intermediates manufacturing company2. Working as per SOP and follow the safety protocols3. Working experience in GMP environment4. Maintaining Documentation / BMRGood Manufacturing Practices (GMP) are a system ensuring products like food, drugs, and cosmetics are consistently made and controlled to quality standards, minimizing risks like contamination and ...
2 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 2.00 LPA
Key Responsibilities
Assist in implementation and monitoring of GMP, SOPs, and quality systems
Support preparation, review, and control of QA documentation
Assist in batch record review and compliance checks
Participate in internal audits and inspection readiness activities
Support handling of deviations, change controls, and CAPA
Assist in raw material, in-process, and finished goods release documentation
Coordinate with ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 5.00 LPA
The HR Assistant Manager is responsible for leading end-to-end HR operations, ensuring strict adherence to statutory and pharma-specific regulatory compliances, and managing the employee lifecycle within a high-stakes manufacturing or R&D environment.
Key Responsibilities
Talent Acquisition & Workforce Planning: Lead recruitment for specialized API roles including R&D, QA, QC, Production, and Supply Chain. ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
1.80 LPA TO 2.40 LPA
A Batching Operator runs machinery to mix ingredients (like cement, chemicals, or food items) precisely according to formulas, ensuring quality and safety by monitoring processes, conducting tests, managing inventory, performing basic maintenance, and keeping detailed production records, all while adhering to strict safety and GMP (Good Manufacturing Practices) standards for accurate, ...
3 Opening(s)
15.0 Year(s) To 25.0 Year(s)
15.00 LPA TO 20.00 LPA
To review and implement a Quality Management System for cGMP compliance at the Production (Injectable) plant.
To prepare, Review and Approve BMR, BPR and related documents.
Handling of Caliber QAMS, DMS, Nichelon 5 CMS, Dynamic, Schedule and Track and trace Serialization & aggregation.
Giving the required training also Responsible for Media fill and ...
18 Opening(s)
3.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 24.00 LPA
Job Details:
Job Title: Machine operator
Experience: Minimum 3 years
Location: Mwanza, Tanzania
Job responsibilities:
Lubricate grease to high movable parts of the machine.
Arrange all raw material to WIP for production facilitation.
Arrange all packaging material to WIP for production facilitation.
Carry out daily, monthly and annual preventative Maintenance of all machines in the preform plant.
Ensure all machines are safe and ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
3.50 LPA TO 4.50 LPA
Key Responsibilities
Operate and manage Injection Moulding Machines efficiently and ensure smooth production flow.
Execute daily, weekly, and monthly production plans as per requirements.
Assist the Production Manager in implementing corrective and preventive actions based on IPC test results and customer complaints.
Coordinate with area supervisors and other departments to ensure all related activities ...
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 ...