Validation Specialist

27 Mar 2024

Vacancy expired!

Job Description:
  • 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.
  • 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.

Required:
  • 6 plus years' experience
  • 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

Skills:
  • Application Periodic Review: 3 to 5 years
  • Computer System Validation: 3 to 5 years
  • HP ALM: 3 to 5 years
  • Problem Investigations: 3 to 5 years

  • ID: #49559806
  • State: Florida Tampa bay area 33601 Tampa bay area USA
  • City: Tampa bay area
  • Salary: USD TBD TBD
  • Job type: Permanent
  • Showed: 2023-03-27
  • Deadline: 2023-05-25
  • Category: Et cetera