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)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 7.00 LPA
Position: Shift Incharge - Production
Location: Uppugal - Warangal
Experience: 5 - 10 Years
Industries: Oil
Responsibilities:
Monitor processes and ensure production and product complies to set standards and specification
Responsible for productivity of all plants and ensure the set targets are met
Ensure measures such as preventive and predictive maintenance schedules ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: Production Officer
Location: Daman
Experience: 1 - 5 Years
Industries: Pharma
Responsibilities:
Monitor and control daily production activities as per production plan.
Ensure manufacturing of tablets, capsules, syrups, or other formulations as per SOPs and GMP guidelines.
Supervise machine operation, line clearance, and production manpower.
Maintain batch manufacturing records (BMR) and production ...
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, ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Responsibilities: QA Executive
To assign control number of Change control, Deviation, CAPA, OOS, OOT etc.
To handle QMS related documents and its applicable Quality trends.
To review investigation reports for deviation, OOS, OOT, OOE & Market Complaint.
To coordinate for Internal Audit.
To Issue and retrieve of Batch Production Record and Equipment Cleaning Record for ...
1 Opening(s)
1.5 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Roles & Responsibilities – Warehouse Executive (API Pharma)
Handle receipt, storage, and issuance of Raw Materials, Solvents, and Finished Goods.
Maintain inventory records and ensure stock accuracy.
Follow FIFO/FEFO practices for material management.
Prepare and maintain warehouse documentation (GRN, Issue Slips, Stock Registers, etc.).
Coordinate material issuance to Production as per requirements.
Conduct physical stock verification ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Quality Executive(Documentation)
Location: Dadra & Nagar Haveli - Slivassa
Experience: 6 - 8 Years
Industries: Cosmetic
Responsibilities:
Monitor and maintain quality standards across manufacturing and operational processes.
Perform inspections of raw materials, in-process products, and finished goods.
Review and maintain quality documentation, SOPs, specifications, and ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 12.00 LPA
Position: Asst. Manager/Manager - QC
Location: Ankleshwar
Experience: 8 - 10 Years
Industries: Chemical
Responsibilities:
Quality Control Operations
Oversee day-to-day quality control activities for raw materials, in-process products, and finished goods.
Ensure compliance with quality standards, SOPs, and customer specifications.
Monitor inspection and testing procedures to maintain product quality.
Approve or reject materials/products based ...
1 Opening(s)
7.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 14.00 LPA
- Maintain overall upkeep of plant equipment
- Review, plan, and execute preventive maintenance
- Troubleshoot plant machinery and facility challenges
- Review work orders and ensure compliance within timelines
- Ensure facility integrity and hygiene standards (GMP compliance)
- Optimize facility maintenance work orders and manage change compliance
- Execute facility integrity plans aligned with ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 7.00 LPA
Key Responsibilities
Monitor daily production activities and ensure quality compliance.
Conduct in-process quality checks and finished goods inspections.
Maintain QA documentation, reports, SOPs, and records.
Ensure compliance with GMP, HACCP, FSSAI, and food safety standards.
Handle customer complaints and implement corrective actions.
Coordinate with Production, QC, and Store departments.
Conduct hygiene audits and ensure sanitation standards.
Monitor raw ...