Job Description
1.Preparation and review of SOPs.
2.Review of documents related to Formulation department, Analytical department and Quality Assurance department.
3.Review of log books and laboratory note books.
4.Issuance, retrieval and archival of formats, laboratory note books and log books.
5.Review of Qualification and calibration documents.
6.Technology transfer activity.
7.Issuance, retrieval and archival of documents.
8.Allocation of instrument and equipment identification number.
9.Management of training system.
12.Internal audit
13.Licensing and permission activities with local regulatory
14.Stability sample management
15.Qualification and Calibration of stability chambers.
Male candidate
Working Monday to Friday
9 pm to 6.30
Location: sanand(Ahmedabad)
Please note company has pick and drop facility to plant.
Can share more details on mail/Call
Share CV on [Confidential Information]
91-9537555***
Employement Category:
Employement Type: Full time
Industry: Pharmaceutical
Functional Area: Quality Control
Role Category: Other - Quality Assurance
Role/Responsibilies: Quality Assurance
Contact Details:
Company: UpMan Placements
Location(s): Ahmedabad