1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 4.80 LPA
Position: Executive/Asst. Manager - Production
Location: Silvassa
Experience: 2 - 10 Years
Industries: Pharma
Responsibilities:
Manage day-to-day production operations, ensuring timely and efficient manufacturing.
Ensure compliance with GMP, safety, and environmental regulations.
Optimize production processes to improve efficiency, reduce costs, and maintain product quality.
Monitor and control production schedules, ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 4.20 LPA
Position: Executive/Asst. Manager - QA
Location: Silvassa
Experience: 2 - 10 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management ...
2 Opening(s)
7.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
a) Should have at least 7+ years of work experience out of which minimum 5+ years of experience shall be in Business Excellence.
b) Should be a certified six sigma black belt/Green Belt.
c) Should be a B.E/ B. Tech in Engineering (any branch) or MBA.
d) Should be EFQM certified professional having ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 8.00 LPA
Position: Executive/Sr. Executive - Production
Location: Daman
Experience: 5 - 10Years
Industries: Pharma
Responsibilities:
Manage day-to-day production operations, ensuring timely and efficient manufacturing.
Ensure compliance with GMP, safety, and environmental regulations.
Optimize production processes to improve efficiency, reduce costs, and maintain product quality.
Monitor and control production schedules, inventory ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QA Officer
Location: Daman
Experience: 1 - 2 Years
Industries: Pharma
Responsibilities:
Line Clearance before the start of the Production activities.
Performing & Recording In-Process Checks of Manufacturing & Packing department.
Monitoring dispensing of Raw material and packing materials.
In-house Calibration of IPQC Instruments (as per Frequency).
Checking of stage ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
3.50 LPA TO 7.50 LPA
Job Title: Production Manager.
QUALIFICATION: B.sc , Msc ,B. Pharma, M.Pharma .
Experience 10 years.
SALARY : 60 TO 70K.
TIMING : 9 TO 6PM.
Location: Odd, Pirana, [Ahmedabad ]
Job Type: [Full-time]
Job Summary:
Production planning Materials procurement BMR/BPR prepare and executed Man Power arrangement Related documents and practical work Production manager for tablet and capsules
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: Executive - QA
Location: Vapi
Experience: 2 - 4 Years
Industries: Pharma
Responsibilities:
BMR and BPR review and get corrected as per requirement.
Periodic review of SOP for stamping , change control ,execution and distribution activity, if change control then inform to reporting head.
Raw material , packing ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
25.00 LPA TO 30.00 LPA
Position: QA Manager
Location: Ahmedabad
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management Systems (QMS) as per USFDA, WHO-GMP, ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
7.20 LPA TO 8.40 LPA
Position: Production Manager
Location: Ahmedabad
Experience: 10 - 12 Years
Industries: Pharma
Responsibilities:
Should have worked as a production manager having experience either in tablets or in liquids
Should have faced international audits, should be working in WHO company
Should have some basic acumen towards worker management
Should have mindset towards importance and implementation of ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
Monitoring all processes in process & FG quality results and trends
Reporting periodic status on quality function periodically and formats as defined to operations and top management
Maintaining all documents as defined for integrated QMS/ EMS/ TS
Undertaking RCA for recurring failure of processes / products followed by evolving CAPA in consultation with ...