400 Job openings found

1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 13.00 LPA
Position:          Dy. Manager - Quality Location:         Vapi Experience:      8 - 10 Years Industries:       Pharma API  Responsibilities: Quality Management System (QMS)   Establish, implement, and maintain an effective Quality Management System in line with cGMP, ICH, USFDA, EU-GMP, WHO, and other regulatory requirements. Ensure compliance with SOPs, policies, and ...
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, ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 7.00 LPA
Job Description – R&D Parenteral (Formulation) Specialist Company: Concept Pharma Pvt. Ltd. Position: R&D Parenteral (Formulation) Specialist Experience: 2–5 Years CTC (Budget): Negotiable Location: Aurangabad Key Responsibilities Support the R&D team in formulation development of parenteral products, including Small Volume Parenterals (SVP) and Large Volume Parenterals (LVP) in both powder and liquid dosage forms. Perform sterile ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position:          QA Officer Location:         Sarigam Near By Vapi Experience:     3 - 6 Years Industries:      Chemical Responsibilities: Ensure current versions of all GMP documents are in use across departments. Prepare, revise, and control SOPs and related quality documents. Implement and enforce Good Documentation Practices (GDP). Prevent retention of obsolete ...
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 ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.50 LPA TO 3.25 LPA
Job Title: Production Planning & Control (PPC) Executive – Pharma Location: Aurangabad CTC: ₹Negotiable Experience: 1–2 Years Industry: Pharmaceutical Manufacturing Job Summary We are looking for a Production Planning & Control (PPC) Executive with strong IT and analytical skills to support production planning, scheduling, and coordination activities in a pharmaceutical manufacturing environment. The ...
1 Opening(s)
15.0 Year(s) To 18.0 Year(s)
15.00 LPA TO 20.00 LPA
Position:         Project Head Location:        Khopoli - Raigarh Experience:     15 - 20 Years Industries:      Pharma    Responsibilities: Lead end-to-end execution of greenfield pharmaceutical formulation projects from concept to commercial production. Define project scope, timelines, budgets, and resource plans aligned with business objectives. Oversee facility design, layout, utilities, cleanrooms, and equipment selection ...
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 ...

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