161 Job openings found

1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
5.00 LPA TO 8.00 LPA
Responsibilities: QA Executive   Lead and manage the Quality Assurance department and ensure compliance with quality standards. Develop, implement and monitor QA systems, SOPs, specifications and quality procedures. Oversee raw material, in-process and finished product quality and ensure timely release. Handle customer complaints, CAPA, deviations, investigations and root cause analysis. Coordinate internal, external and customer audits ...
1 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 2.20 LPA
Position:          QC Chemist Location:         Jhagadia nearby Ankleshwar Experience:      0 - 1 Years Industries:       Chemical Responsibilities:         Responsible for Documentation work in QC Department Candidate must have knowledge of HPLC & GC  Responsible for manufacturing the batch as per MOM or BMR. Shall maintained all records related to manufacturing Overall looking after the ...
1 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 3.00 LPA
1.0     Packing Activities.       1.1 Packing as per order given by marketing team.     1.2 Ensure Grade wise packing.     1.3 Take packing material for packing which is approved by QA and QC.   2.0    Supervision and Coordination of Shipment.      2.1 Confirm shipment.    2.2 Confirm requirement of packing type.            2.2.1 Ensure availability or minimum ...
3 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...
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)
2.0 Year(s) To 3.0 Year(s)
Not Disclosed by Recruiter
Role Summary Manage SAP operations, Loan License (LL) compliance, new product certification, and supply chain coordination for the Generics business, ensuring audit readiness, timely launches, and uninterrupted product supply. Key Responsibilities Manage SAP MM & PP transactions, process orders, inventory, and material movements. Coordinate with Supply Chain, QA, Manufacturing & Logistics for timely product ...
10 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
Shift In-Charge – Production | Aroma Chemicals Department: Production Reports To: Production Manager / Plant Head Location: Manufacturing Plant Experience: 4–8 Years Qualification: B.Sc/M.Sc Chemistry or Diploma/B.E./B.Tech Chemical Engineering Job Responsibilities: Manage overall shift-wise production activities and achieve production targets. Supervise reactor operations, reaction, distillation, filtration, extraction & drying processes. Monitor critical process parameters as per ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Responsibilities: Online quality checking & FG To give feedback to production & Quality Department regarding online deviations and get the corrective actions To maintain all documentations as per IPQA To help operations maintain GMP Preparation of the In Process analysis reports for QC To lead and monitor IPQA activities in the Pre dispatch samples sending, communication ...
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)
4.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
A Quality Assurance (QA) Assistant Manager for a starch powder or pharmaceutical/food-grade starch active/derivative manufacturing plant in the Dhule/Dondaicha MIDC region oversees cGMP compliance, QMS documentation, process validation, and regulatory audits for specialized grades (IP, BP, USP).    Job Profile & Core Details Position Title: Assistant Manager - Quality Assurance (QA) Industry Segment: ...

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