1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
25.00 LPA TO 30.00 LPA
Position: GM Operation
Location: Guwahati
Experience: 15 - 20 Years
Industries: Pharma
Responsibilities:
Oversee end-to-end manufacturing operations for Tablets, Capsules, Softgels, and packaging activities to achieve production targets while maintaining quality and delivery timelines.
Ensure strict compliance with cGMP, WHO-GMP, regulatory requirements, SOPs, and applicable national and international guidelines.
Lead and coordinate with QA, QC, ...
1 Opening(s)
12.0 Year(s) To 16.0 Year(s)
20.00 LPA TO 24.00 LPA
Position: Sr. Manager - Production
Location: Bhopal
Experience: 12 - 16 Years
Industries: Pharma
Responsibilities:
Lead overall Production operations for pharmaceutical injectable manufacturing
Manage and ensure smooth execution of cartridge filling operations
Plan and monitor production schedules to achieve targets as per quality standards
Ensure compliance with GMP/cGMP, SOPs and regulatory requirements
Oversee ...
1 Opening(s)
0 To 1.0 Year(s)
1.20 LPA TO 1.80 LPA
The Asst Production Chemist is responsible for planning, supervising, and executing manufacturing activities to ensure products are produced safely, efficiently, and in compliance with cGMP, ISO 13485 (where applicable), Medical Device Rules (MDR) 2017, approved procedures, and company quality standards. The role includes manpower supervision, production planning, documentation, equipment utilization, ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
9.00 LPA TO 10.00 LPA
Position: QA Executive
Location: Daman
Experience: 8 - 10 Years
Industries: Pharma
Responsibilities:
Ensure compliance with cGMP, GLP, SOPs and regulatory requirements.
Review and approve BMR/BPR, SOPs, specifications and quality documents.
Handle Deviations, OOS/OOT, CAPA, Change Control and investigations.
Monitor QA activities across manufacturing and ensure GMP compliance.
Conduct and support internal, customer and ...
1 Opening(s)
12.0 Year(s) To 18.0 Year(s)
15.00 LPA TO 18.00 LPA
Assistant Manager – Production Jobs in Sonipat | Orbit Global HR Consultants
Assistant Manager – Production Jobs in Sonipat are now open through Orbit Global HR Consultants LLP, one of the leading Food Manufacturing Recruitment Agencies in India specializing in executive search, plant leadership hiring, production, operations, quality, supply chain, engineering, ...
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1 Opening(s)
0 To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Officer/Executive - Production
Location: Silvassa
Experience: 0 - 5 Years
Industries: Pharma
Responsibilities:
Execute daily production activities as per the approved production plan and batch schedule.
Ensure manufacturing of cosmetic and pharmaceutical products in compliance with GMP, SOPs, and quality standards.
Supervise dispensing, manufacturing, filling, packing, and batch changeover ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 8.00 LPA
Position: Dy. Manager - QC
Location: Vapi
Experience: 6 - 8 Years
Industries: Pharma - API
Responsibilities:
Manage day-to-day Quality Control activities for raw materials, intermediates, APIs, finished products, and stability samples.
Ensure compliance with cGMP, GLP, ICH, FDA, EU GMP, and regulatory requirements.
Review and approve analytical test results, ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Description:
Position: Asst/Dy. Manager – Manufacturing
Location: Slivassa
Experience: 8 - 10 Years
Industries: Cosmetic
Responsibilities:
Always maintain good hygiene and housekeeping in all manufacturing areas, ensuring adherence to personal hygiene, GMP, and safety standards.
Manage production planning, workflow optimization, and effective resource allocation.
Prepare and execute the daily manufacturing ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 12.00 LPA
Job Summary
We are seeking an experienced Greenfield Project Manager to lead the establishment of a new pharmaceutical manufacturing facility from project initiation to commissioning. The candidate will be responsible for overseeing construction activities, ensuring compliance with pharmaceutical regulatory standards, coordinating machinery installation, and supporting facility readiness for operations.
Key Responsibilities
Project Planning ...
10 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 6.00 LPA
Key Responsibilities
Knowledge of GDP & GMP documentation and compliance.
Preparation and handling of Investigation Reports, Complaint Reports, and related documentation.
Preparation of SOPs, BPRs, ECRs, Qualification Protocols, and Reports.
Sound knowledge of SAP and DMS systems.
Proficient in MS Word, Excel, and PowerPoint with good typing speed.
Handling of Deviation, Change Control, Complaints, Risk Assessment, ...