1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.50 LPA
Prepare and send price quotation to drilling companies and drilling contractor’s bases on customer enquiries.
Visits customer’s offices and project site to discuss and conduct inspection to verify details of the enquiries.
Prepare work in progress report and send to customers.
Coordinates with customers and forwarding companies regarding delivery or collection of equipment ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
9.00 LPA TO 11.00 LPA
Assisting the senior doctors in checking the patients.
Diagnosis the disease as per symptoms.
Observing and performing the examination of samples for disease and diagnose.
Periodically meeting the patients and observing their improvement.
Assisting senior doctors in checking the patient
Diagnosing the disease as per symptoms
Observing and Performing the examination of samples for disease diagnose ...
2 Opening(s)
5.0 Year(s) To 15.0 Year(s)
3.00 LPA TO 6.00 LPA
Responsible for Accounts Payable, Accounts Receivable and Payroll Administration and Admin Activities.
Maintained the General Ledger encompassing UP and Delhi region.
Prepared internal and external financial and tax statements for review by corporate and external Audit Teams.
Maintain and reconciliation of bank accounts.
Responsible to maintain reconciled statement and reminding letters for all accounts ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
5.50 LPA TO 7.00 LPA
Candidate must have experience in production assembly with qualification in B.Tech Mechanical or CIPET
Production in Assembly controlling all the production activities
Continual improvement in production processes for:
Maximum utilization of all resources
To achieve maximum production target
For complete customer satisfaction in terms of quality & cost
Development in Process for better efficiency
Production Line setting ...
1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
7.20 LPA TO 8.40 LPA
Preparation of Certificate of Pharmaceutical Product.
Expertise in liaising, coordinating inspections with regulatory agencies (FDA ISO 9000)
Knowledge of Microsoft Office, Microsoft Excel, ERP etc.
Goal Oriented and Results Driven Team Leader.
Expertise in writing, reviewing & approving lab procedures / documentations, Out off Specification reports, batch records, protocols, etc.
Review of QC related ...
3 Opening(s)
3.0 Year(s) To 4.0 Year(s)
2.50 LPA TO 3.00 LPA
Bulk & Finished Products analysis by UV-VIS Spectrophotometer.
Prepare Analysis Report of Bulk Products.
Prepare COA of Finished Products.
Raw Material analysis.
Calibration of Ultraviolet
Calibration of pH meter.
Operate HPLC.
Calibration of HPLC.
Responsible For all Activity of Q.C Department ,cGLP as per 21(CFR)part 11,DRA documents for export,
Ensure and review,Approval of R.M Finished Products and Stability of ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.80 LPA TO 6.00 LPA
Identifying potential organization for our company’s product range to get desired insights.
Confer with customer and/or their engineers to assess equipment needs and to determine system requirements and act as a primary business contact for the customer.
Recommend improved machinery to existing customers, showing how changes will lower costs of service/production.
Advising & ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.10 LPA TO 3.60 LPA
Receiving Monthly & daily Production plan from Production Manager.
Manufacturing of batch as per MBR.
Temperature & Relative Humidity monitoring in manufacturing area.
Maintaining logbooks(General cleaning logbook,Equipment calibration & cleaning logbook,).
Preparation of daily production & manpower Record.
Online the Batch Manufacturing Record (BMR).
In process checks of all stages of manufacturing & packing of Tablet, ...