COMPUTER SYSTEM VALIDATION SPECIALIST PRINCETON, NJ
Required Skills:
Must Haves:
5+ years of experience in managing the projects as CSV specialist /lead.
5+ years of experience in testing , (script reviewing from a QA perspective in particular )
5+ years of experience in authoring , reviewing various validation documentation such as (Val plan , Risk assessments etc.)
Good communication and writing skills.
Data Integrity experience is a plus.
6+ years' experience
Advanced knowledge of complete MS Office suite and Visio. Firm understanding of technology platforms as needed for project.
Experience with electronic document management systems (e.g., documentum, Qumas, SharePoint etc.); application development and lifecycle management (e.g., HP ALM, JIRA, etc.); and IT service management systems (e.g., ServiceNow, SAP Solution Manager, etc.)
Excellent oral and written communication skills in English. Strong expertise and ability to interview and accurately interpret communication requirements of team members. Once trained, have the ability to work independently on CSV projects with minimal oversight.
Ability to perform in a highly matrixed organization structure.
Project Description:
Apply FDA, MHRA, and other applicable global health authority regulations to the development of computer systems supporting regulated business processes.
Follow SOPs and industry best practices.
Possess Expertise on Good Documentation and Good Testing Practices, in order to train those within the business that are less familiar.
Facilitate the Computer system Validation Risk Assessment to identify governing regulations and validation deliverables during the development of the computer system.
Review validation deliverables for projects which are contracted to third party suppliers.
Maintain close communication with stakeholders and team members to keep apprised of computerized system needs, impacts on computer validation, project validation status, and other relevant issues.
Assist in planning, implementing, and documenting user acceptance testing.
Review computerized systems validation documents such as:
Requirements Specification
Design Specification
CSV Risk Assessment
Test Plans
Test Summary Reports
Data Migration Plan
Pre/Post Executed Test Scripts
Traceability Matrix
Release to Production Statements
Direct and review testing
Provide guidance on quality issues that affect the integrity of the data or the system.
Obtain and respond to QA review.
Participate in establishing standard quality and validation practices.
Independently assess compliance practices and recommend corrective actions.
Approve validated computer system related change requests.
Monitor regulatory and inspection trends and advise the business on suitable action.
Ability to create documents to an existing document standard.
Able to develop all documentation required for a 21 CFR Part 11 validated project, including Validation Plans and Summaries.
This 6+ month position starts ASAP.
Please E-MAIL your resume (attachment to email) with rate and availability to Cheryl:
ALPHA'S REQUIREMENT #21-01135 MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE #ZR #LI-CA1
