1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
14.00 LPA TO 20.00 LPA
Position: Manager - QC
Location: Sarigam near by Vapi
Experience: 15 - 20 Years
Industries: Chemical
Responsibilities:
QC management and planning
Ensure that the test methods are updated and validated.
Overview / monitoring of analysis of Raw materials and Finish Goods.
Chemicals /glassware inwards and instrument procurement require for analysis.
Responsible for the timely ...
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 ...
5 Opening(s)
0 To 5.0 Year(s)
1.50 LPA TO 5.00 LPA
🔹 Key Responsibilities:
Execute day-to-day operations in aseptic and sterile manufacturing areas
Monitor LVP production activities in compliance with SOPs, cGMP, and regulatory guidelines
Operate and maintain critical equipment including autoclaves, filling machines, and sterilizers
Ensure strict adherence to safety, quality, and environmental standards
Prepare, review, and maintain batch production records and related documentation
🔹 Qualifications ...
1 Opening(s)
0 To 0
0.00 LPA TO 2.16 LPA
QC (Quality Control) Chemist fresher ensures raw materials, in-process samples, and finished goods meet quality, safety, and regulatory standards through routine laboratory testing and documentation. Key duties involve conducting wet chemistry tests, utilizing analytical instruments, preparing reports, and maintaining strict compliance with cGMP/GLP standards.
Key Responsibilities & Duties:
Testing & Analysis: Perform routine testing ...
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 ...
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)
7.0 Year(s) To 10.0 Year(s)
4.80 LPA TO 7.20 LPA
JOB DESCRIPTION
20.12.25
122339
HPS/2025/670
Production Manager/Pharma
Male
1
7 to 10
B.Pharma /D.Pharma
8 Hours
A Pharma Production Manager oversees daily manufacturing, ensuring products meet strict quality (cGMP) and safety (EHS) standards, managing teams, optimizing schedules, controlling costs, and handling documentation
Key Responsibilities-
Production Planning & Execution: Schedule daily/weekly production, manage resources (materials, manpower), and execute plans to meet targets efficiently.
Quality & Compliance: Enforce ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 6.00 LPA
Production Management: Supervise and coordinate all shift production activities, ensuring adherence to the planned schedules and achieving production targets. This includes monitoring process parameters, raw material usage, yields, and overall operational efficiency.
Quality and Compliance Assurance: Ensure strict compliance with cGMP (current Good Manufacturing Practices), Standard Operating Procedures (SOPs), and other regulatory guidelines ...
3 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.60 LPA TO 3.60 LPA
Perform routine calibration and maintenance: Conduct periodic preventive maintenance, testing, and calibration of all instrumentation equipment (including sensors, transmitters, and control valves) according to manufacturer specifications and relevant industry standards (e.g., ISO, NABL, cGMP).
Troubleshoot and repair instrumentation systems: Diagnose, analyze, and repair defects or malfunctions in complex control systems, including Programmable Logic ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.00 LPA
Key Roles and Responsibilities
In the pharmaceutical industry, a Project Engineer's main responsibilities involve ensuring the technical work is completed safely, on time, within budget, and in compliance with stringent regulatory standards (like cGMP).
Project Planning & Execution
Prepare & review project schedule, P&ID, and GA Drawing.
Co-ordinate with cross functional teams. (Civil, ...