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CSV Lead at Remote, Remote, USA
Email: [email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=1038743&uid=

From:

Preety Sharma,

HMG America

[email protected]

Reply to:   [email protected]

Greetings!

HMG America LLC is the best Business Solutions focused Information Technology Company with IT consulting and services, software and web development, staff augmentation and other professional services. One of our direct clients is looking for Technical Lead in North Carolina, Raleigh. Below is the detailed job description.

Title:  Technical Lead

Location:  North Carolina, Raleigh onsite 

Duration: 12 Months

Mandatory Skills:  CSV, Computer System Validation, Clinical Systems

Job Description:

Keywords:   CSV, Computer System Validation, Clinical Systems, Safety Systems, Infrastructure Qualification, 21 CFR part 11, GAMP 5, ICH, EMEA, MHRA regulations

Roles and Responsibilities

Must Have
10 +  years  Experience in Validating GxP applications
 Experience in FDA and/or Global regulated environment with good understanding of GCP , GLP and Risk based validation strategy
  Provides consultation and counseling on Risk and Compliance module implementation in reference to regulatory quality
  Support Risk assessment
  Document Regulatory Requirements and Review Specification documentation (viz. User Stories, URS, FRS)
  Review and final Approval of requirements, Technical Design and Solution Architecture Plan, IQ, OQ and PQ pre and post execution documents
  Lead, Write, Review/ Approve Discrepancy Logs (final dispositions)
  Lead, Write, Review / Approve Requirement Traceability Matrix (RTM) and Validation Summary Reports
Good to Have (secondary skills)
  Experience in Clinical systems like CTMS, CDMS, EDC, Veeva Vault, QMS and Safety Systems and Infrastructure Qualification
  Conduct Periodic Reviews of GxP Apps as per the frequency stated in the governing SOP and write Periodic review reports and Review and Approve Periodic Review Reports
  Tracks the Periodic review findings and open CAPA s to a closure
  Review and Approve System Support and Operations plan
  Participate in and support Audits.
  Contribute and Review/ Approve Decommissioning Plans & Decommissioning Reports
  Contribute, Review/ Approve deliverables for Change Management Support
  Maintain validation documentation throughout product lifecycle viz.as a result of Change, Periodic Review, Audits
Communication
  Immaculate communication and handles multiple clients/ projects
  Works in Consulting capacity

(1.)  To ensure process improvement and compliance, and participate in technical design discussion and to review technical documents (2.)  Co-ordination with On-Site Engineers and attending customer calls (3.)  Raising risks, issues and escalation to senior management and customer (4.)  To create all quality documents, collect metrics data and conducting Audits. To perform Value creation and KM activities. (5.)  To create project plans and keep track of schedule for on time delivery as per the defined quality standards

Keywords: information technology Colorado
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=1038743&uid=
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01:16 AM 23-Jan-24


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