1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
12.00 LPA TO 12.00 LPA
Job Title: Assistant Manager – Quality Assurance (Pet Food)
Job Summary
The Assistant Manager – Quality Assurance will be responsible for implementing and maintaining the Quality Management System (QMS), ensuring compliance with food safety standards, supporting new product commercialization, managing documentation, and coordinating with R&D, manufacturing, and third-party manufacturers to ensure consistent product quality and ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 3.60 LPA
Position: Officer/Executive - Production (U-1)
Location: Daman
Experience: 2 - 6 Years
Industries: Pharma
Responsibilities:
Handle day-to-day production activities as per production plan.
Operate and monitor reactors, centrifuges, dryers, and other process equipment.
Follow Batch Manufacturing Record (BMR) and Standard Operating Procedures (SOPs).
Monitor process parameters such as temperature, pressure, and reaction time.
Ensure proper charging ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QA Officer.
Location: Daman
Experience: 1 - 3 Years
Industries: Pharma
Responsibilities:
Ensure compliance with cGMP, GLP, and regulatory requirements.
Review and approve Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and analytical reports.
Handle deviations, change controls, CAPA, OOS, OOT, and risk assessments.
Conduct line clearance, in-process checks, and shop ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
Perform line clearance and in-process checks.
Ensure compliance with cGMP, GDP, and SOP requirements.
Handle deviations, change control, CAPA, OOS, and OOT investigations.
Prepare, review, and update SOPs and QA documents.
Conduct GMP audits and shop floor inspections.
Monitor documentation and maintain data integrity.
Coordinate with Production, ...
50 Opening(s)
2.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 5.00 LPA
Operate primary packing machines such as:
Blister Packing Machine
Strip Packing Machine
Bottle Filling Line
Cartoning Machine
Leak Test Machine
Perform machine setup, changeover, and line clearance activities.
Ensure packing activities are carried out as per BMR/BPR and SOP guidelines.
Monitor machine performance and minimize breakdowns and rejection.
Maintain production targets with required quality standards.
Check batch coding, foil printing, ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
7.00 LPA TO 8.00 LPA
Role: Batch Manufacturing Designation: Executive/Sr.
Executive
Cost Center (E-Mis)*:Reporting Manager Role: Plant Head No. of Reportees: Nil
Role: Key Job responsibilities:1) 3-4 years of prior experience in Beauty and Personal Care Manufacturing (e.g., especiallyShampoo, cream, lotion, conditioner etc.).2) Thorough understanding of batch manufacturing process with knowledge of batch makingsequence, control points and critical ...
10 Opening(s)
2.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 8.00 LPA
🔹 Job Purpose
To perform and monitor granulation activities in solid oral dosage (OSD) manufacturing while ensuring compliance with cGMP, safety, and quality standards.
🔹 Key Responsibilities
⚙️ Production / Operation
Operate granulation equipment such as RMG, FBD/FBE, blender, etc.
Execute wet / dry granulation processes as per BMR (Batch Manufacturing Record)
Set machine parameters and ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 14.00 LPA
Position: Asst./Dy. Manager - Production
Location: Vapi
Experience: 10 - 15 Years
Industries: Pharma - API
Responsibilities:
Production Planning & Control
Execute production plans in line with monthly/weekly schedules.
Monitor batch progress and ensure adherence to timelines and yield targets.
Optimize manpower, equipment, and resources for efficient operations.
Coordinate with PPC/Management for any ...
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 ...
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 ...