Job Description
COMPUTER SYSTEMS VALIDATION CONTRACT ENGINEER required by CareerWise Recruitment for our BioTech client in Limerick, initial 12 month contract on offer.The COMPUTER SYSTEMS VALIDATION CONTRACT ENGINEER will validate/qualify computer systems, including process automation systems, IS applications/infrastructure, and enterprise systems. They also plan, coordinate and participate in a compliant validation process for quality information technology and automation systems which require formal validation documentation under appropriate regulatory requirements and company manufacturing standards.
Role of this position
1. Prepares/reviews validation documentation related to projects/change controls.
2. Manages change controls and other compliance related tasks e.g. non-conformances.
3. Participates in the review of current and future CSV procedures and polices
4. Analyzes the results of testing and determines the acceptability of results against predetermined criteria.
5. Investigates and troubleshoots problems which occur and determines solutions or recommendations for changes and/or improvements.
6. Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation, and maintenance of the procedures, actions, and documentation necessary to ensure compliance within the operation.
7. Coordinates with other departments or outside contractors/vendors to complete validation tasks.
8. Participates in regulatory audits and communicates company's computer validation policies.
9. Assesses company's computer systems and identifies any potential Part 11 or Annex 11 gaps.
10. Manages projects and prepares status reports using Microsoft project and other communication tools.
11. May supervise, lead, or manage lower-level personnel.
JOB REQUIREMENTS
12. Requires BS/BA in Engineering, Chemistry, or Life Sciences with 5+ years of related experience within the fields of Automation and Computer systems and IT Infrastructure Qualification/validation; will substitute relevant experience for education.
13. Experience in a GMP environment essential.
14. Biologics experience highly desirable