Computer system validation engineer

Job Category:
QA/Tester
Job Type:
Contract
Level of IT Experience:
1-5 Years
Area:
North Ireland
Location:
Cavan
Salary Description:
Negotiable
Posted:
13/02/2018
Recruiter:
FRS Recruitment
Job Ref:
FRS27092

Senior Validation Engineer required to review the computer system Validation processes and procedures for the overall site, GxP Risk Management process and ensure that appropriate mitigation steps are implemented to meet current GxP regulations

The systems are as follows

Enterprise resource planning business system (ERP) SAP Business 1 .

QC Empower laboratory chromatography data management system. CDS.

Retrospective validation/Gap analysis of all other potential GxP computer systems on site.

Main Duties & Responsibilities:

Manage the computer system Validation process for the overall site.

Manage GxP Risk Management process and ensure that appropriate mitigation steps are implemented to meet current GxP regulations

Plan and manage the cGMP validation test and documentation phase of the implementation with risk analysis used to define critical GMP components to be validated

Prioritize qualification activities in line with the project schedules and business needs.

Develop templates as required for Validation documentation

Prepare reports of executed protocols for review.

Generate SOP's / other documentation as applicable

Manage all Validation documentation created from the process

Manage overall signature process for all documentation

Manage Validation change control on the project

Develop procedures and processes for the complete computer validated state lifcycle, Data Integrity, Audit Trail review, Disaster recovery etc.

Skills / Experience:

3 - 5 years in a Computerized Systems Validation role (CSV).

Excellent technical English verbal and written skills

CSV experience in an established QA/IT function preferably in the pharmaceutical/healthcare industry

Strong knowledge of GAMP5, CSV, Project Life Cycle and GxP Regulations

Experience drafting, reviewing and/or approving validation documentation VMP, URS, RA, IQ, OQ, PQ, UAT, SAT and VSRs.

Previous experience generating Risk Assessment Matrices for validation projects.

Experience in validating pharmaceutical CDS and ERP system computer/control systems a distinct advantage.

Excellent attention to detail, self-motivated and ability to work to tight or changing deadlines

Work with existing in-house validation team

Contact Details:
FRS Recruitment
Tel: 00353 86 1744576
Contact: Noelle Nagle

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