:

The is as below:

To update and submit Design Review/Design Qualification protocol based on define scope in Work Order, GAD and P&ID;, FS,SDS,SDS, HDS To coordinate with Automation team and review FS,SDS,HDS,FDS, PRINT FORMAT documents based on customer requirement To arrange kick off meeting to explain DR/DQ with detailed scope with Sales/Project and Customers.

To coordinate with Cross functional Team FAT, Production, QC, Planning , Purchase, Service, Sales, Design for further improvement To verify documents with best competitor for further improvement To update FAQ to minimize questionaries' and queries from internal customer and External Customer.





To update Master Standard Protocol Product wise technical data sheet as per Latest regulatory and guideline requirement CE/UL/IBR/ISO for further improvement.

To review and update Design Change Request as discussed in DCR meeting.

To visit at customer site to understand customer requirement for product improvement.

To update Design operational Instructional and Maintenance Manual To present monthly review activity list. Regular activities, Special Achievements and Major challenge activities.

Mon to Sat working days and Office Timing is 8.30 am to 5.00 pm (Adaptable up to 9.00 am)

For further details call Megha on (phone hidden) or you can mail your candidature on [email protected]

📌 Urgent opening for the position of Documentation engineer for pharma machine manufacturing at Ahmedabad (Santej)
🏢 POST A RESUME
📍 Ahmedabad