CSV Document Creation as per the SDLC process and GAMP guideline.
Regulatory Audit support and IT related compliances if any.
Trouble shooting for software application in GxP and Non GxP areas.
Experience in Validating Computer Systems, Software Applications.
Managing all documents in department as a Document Coordinator.
Ensure training is completed on new / revised SOPs as applicable
Citirix Support at server and Desktop Level
Managing and configuration of routers, LAN extender, its etc.
Change Control, Protocol & SOP creation. CSV review and preparation.
Computer System Validations protocol preparation and review as per GMP.
Cloud Base mail Administrator.
Managing IT Compliance with respect to Regulatory requirement and GAMP & cGMP guidelines.
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Employement Category:
Employement Type: Full time Industry: Pharma / Biotech Role Category: General / Other Software Functional Area: Not Applicable Role/Responsibilies: Urgent Requirement -IT Executive
Contact Details:
Company: Ind Swift Labs Location(s): Mohali, Chandigarh
Company ProfileInd Swift Laboratories Ltd.
E-mail : hr.jobs@indswiftlabs.com | Website: www.indswiftlabs.com
Recruiter Name -Aruna ThakurExecutive- HRInd-Swift Laboratories Ltd.Phone NO : +91- 8968374200
Company Info