1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 5.00 LPA
Responsibility:
To maintain the entire documentation as per cGMP and ISO 9001:2015 on daily and fortnightly basis. To supervise the Shift Inspector and Assembly Supervisor. To prepare necessary documentations for new product development trials. Responsible for auditing OPC and preparing the related documents. Responsible to take the trials of new ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 10.00 LPA
Review the Tender documents, drawing, specification, B.O.Q to recognize the scope of Project.
Executing & implementing Project from Kick off to Closing..
Project Scheduling, Monitoring projects and cost control for the successful Project completion.
To prepare and release the Purchase request document for the Project
Vendor follow-up and providing technical clearance ensuring despatch targets ...