|JOB TYPE||Permanent||DATE POSTED||23/09/2019|
Client; Industry leading systems integrator for Automation Systems in the pharmaceutical, food & beverage, utilities, power and built environment markets.
Role Summary; CSV Engineer
Role Requirements: The chosen candidate would typically be accountable for the following activities (but not exclusively): Development of Validation Plans, Installation Qualifications (IQs), Operational Qualifications (OQs) and Summary Reports.
• Prepare, execute, document and report validation protocols in line with GMP’s and other regulatory requirements and standards.
Basic Qualifications: Bachelor of Science/Engineering degree or equivalent.
• Candidates must have demonstrated experience in the delivery and management of IS / Automation systems in addition to a working knowledge of GAMP software development lifecycle, ANSI/ISA-S88 industry standards.
• The successful candidate will have a least 5 years’ experience validating IS Automation systems for manufacturing organizations in the biotechnology or pharmaceutical industries.
Get in touch with us for full brief on this position.
|Charlie Burgess||+442081236574||UK & Ireland||Agency|