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 ...
4 Opening(s)
1.0 Year(s) To 2.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: IPQA Officer.
Location: Daman
Experience: 1 - 2 Years
Industries: Pharma
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess adherence to GMP, standard operating procedures (SOPs), ...
5 Opening(s)
1.0 Year(s) To 2.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Daman
Experience: 1 - 2 Years
Industries: Pharma
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess adherence to GMP, standard operating procedures (SOPs), ...
20 Opening(s)
4.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 6.00 LPA
Position: Engineer/Sr. Engineer - Production
Location: Hajipir - Kutch
Experience: 4 - 8 Years
Industries: Chemical
Responsibilities:
Operate and monitor chemical production processes as per SOPs.
Ensure production targets are achieved with required quality standards.
Handle batch processing / continuous chemical operations.
Maintain process parameters such as temperature, pressure, flow, and ...
40 Opening(s)
2.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 7.00 LPA
Position: Production Executive
Location: Vapi
Experience: 2 - 7 Years
Industries: Pharma - API
Responsibilities:
Prepare the pre-arrangement of batch processing accurately as per the Batch Production Record (BPR) to ensure continuous production without any abstraction.
Take charge of the production area, verifying the process, raw materials, and confirming compliance with the BPR.
Safe ...
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 ...
50 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 10.00 LPA
🎯 Key Responsibilities:
Operate and monitor plant processes through Distributed Control System (DCS)
Handle continuous & batch process operations from control room
Monitor critical parameters like temperature, pressure, flow, level
Ensure safe handling of exothermic reactions / bromination processes
Maintain production targets as per shift plan
Coordinate with field operators for smooth operations
Maintain batch records & ...
3 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 4.00 LPA
🔧 Key Responsibilities
🏭 Plant Operations
Operate and monitor manual batch process plant activities.
Handle unit operations including:
Drying
Mixing
Perform unit processes such as:
Filtration
Pulverization
Manage chemical reactions:
Exothermic reactions
Endothermic reactions
Oversee evaporation and mass transfer operations.
⚙ Equipment Handling
Operate and maintain equipment such as:
Mixture
Reactor
Dryer
Filter
Pulverizer
HAD (if applicable as per plant process)
🛡 Safety & Compliance
Strong knowledge of:
Work Permit System
LOTO / LOTOTO ...
5 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
Qualification & Experience
M.Pharm / M.S / B.S in Chemistry, Pharmaceutics or related discipline
3–5 years of experience in R&D (DQA)
Strong knowledge of GMP, GCP, GLP and 21 CFR 210/211
Experience with dermatology products or medical devices is an advantage
Key Responsibilities
Review development documents, analytical methods, R&D trials, lab notes, PDR, MFR, and batch ...
2 Opening(s)
5.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Job Title
Assistant Manager – Quality Control (Drymix Products)
Department
Quality Control / Quality Assurance
Location
Manufacturing Plant (Drymix / Construction Chemicals)
Reporting To
Manager – Quality Control / Head – QA & QC
Job Purpose
To ensure consistent quality of drymix construction chemical products (Tile Adhesives, Wall Putty, Plasters, Grouts, Repair Mortars, Waterproofing mortars, etc.) by controlling raw ...