1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 7.00 LPA
🔧 Key Responsibilities
Operate tablet compression machines (rotary machines like Cadmach / Fette / Korsch etc.)
Set up machines as per batch manufacturing record (BMR)
Perform in-process checks (weight variation, hardness, thickness, friability)
Ensure proper cleaning of machines and area as per SOP
Handle changeovers and minimize downtime
Maintain production records and logbooks accurately
Follow GMP, safety, ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
12.00 LPA TO 13.00 LPA
Position: Asst./Dy. Manager - Production
Location: Vapi
Experience: 10 - 12 Years
Industries: Pharma - API
Responsibilities:
Oversee day-to-day API manufacturing operations (batch/continuous processes).
Ensure strict compliance with cGMP, USFDA, MHRA, WHO, and other regulatory standards.
Review and execute Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
Coordinate with QA/QC to ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Position Overview
We are looking for a QMS Engineer (Executive) with experience in pharmaceutical formulation (OSD) to manage and maintain the Quality Management System (QMS) in compliance with regulatory requirements such as ICH, WHO-GMP, USFDA, and EU-GMP.
Key Responsibilities
1. Documentation Management
Prepare, review, and control SOPs, STPs, formats, and policies
Ensure proper document lifecycle ...
4 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 2.64 LPA
Description:
Position: Lab Chemist
Location: Vapi
Experience: Fresher
Industries: Automobile
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of GC
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and Procurement of the packing material.
To ensure ...
5 Opening(s)
1.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 LPA
Position: QA Asst Manager ( OSD , ORAL LIQUID & OINTMENT FACILITY) Position: QA Asst. Manager Vacancy: 01 Location: VAPI- GUJARAT Experience: 10 to 15 Years Qualification: B. Pharma / M. Pharma Core Technical Expertise: ï‚· IPQA (In-Process Quality Assurance): Hands-on experience in monitoring manufacturing and packaging processes, line clearance, ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
position: Production Officer
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Location: VAPI- GUJARAT
Experience: 2 to 4 Years
Qualification: B. Pharma / M. Pharma Core
Production Operations o Oversee daily manufacturing activities for tablets and capsules: granulation, compression, coating, encapsulation, and packaging.
Ensure adherence to batch manufacturing records (BMR), batch packing records (BPR), and standard operating procedures (SOPs).
Monitor and optimize production schedules ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
🔑 Key Responsibilities:
✅ Handle complete shift production activities ✅ Monitor batch charging, reaction parameters, filtration, drying & packing ✅ Supervise operators and contract manpower ✅ Ensure adherence to SOP, BMR & safety guidelines ✅ Maintain production logbook & shift reports ✅ Coordinate with QA/QC, Maintenance & EHS departments ✅ Handle ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 8.00 LPA
Position: Sr. Executive - QA
Location: Bhimpore - Daman
Experience: 7 - 10 Years
Industries: Medical Device
Responsibilities:
Preparation, coordination, and successful handling of audits from USFDA, MHRA, WHO-Geneva, and other regulatory authorities.
Review and compilation of documents required for regulatory inspections.
Preparation of ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Sr. Officer - IPQA
Location: Bhimpore - Daman
Experience: 6 - 8 Years
Industries: Medical Device
Responsibilities:
IPQA (In-Process Quality Assurance) Monitoring
Supervise and monitor all IPQA activities in manufacturing areas.
Ensure compliance with cGMP guidelines during production processes.
Line clearance verification before batch ...
1 Opening(s)
0 To 3.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: Production Chemist
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 ...