Job Type: Contract
Job ID: JO-2104-25804
Consultant: Karen McHugh
Do you have at least 5 years’ experience validating IS Automation systems for manufacturing organizations in the biotechnology or pharmaceutical industries?
Do you have experience in the validation of one or more of the following system types from project conception to delivery; DCS/SCADA/MES/Historian?
If you have the relevant experience, send your CV to email@example.com or call Karen on +353 17978720 for a confidential chat.
CSV Lead - BioPharma - Dublin
CSV lead on an Enterprise Cyber Resilience Project which involves migration of Automation Systems, MES and PI to segmented infrastructure.
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.
Assure that all validation test procedures are in line with current technology, corporate and governmental regulations.
Ensure that the Validation Strategy meets the quality requirements of its customers and applicable regulations FDA, EU & International Standards
Review and Approve validation protocols and assessments from a quality system documentation perspective.
Liaise with Engineering / Automation and external vendors regarding equipment documentation, HDS, SDS, FDS, User Requirement Specifications (URS’s), and any other associated validation issues.
Participate and communicate as required in project activities.
Develop procedures to manage computerised systems where required
Develop and present project plans to project management senior staff
Bachelor of Science/Engineering degree or equivalent.
Knowledge of cGMP’s and other worldwide regulatory requirements.
Problem solving ability and excellent oral and written communications skills
Understanding of the computer system validation lifecycle
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 at least 5 years’ experience validating IS Automation systems for manufacturing organizations in the biotechnology or pharmaceutical industries.
Candidates should have experience using a paperless validation system such as HP ALM
Experience in the validation of one or more of the following system types from project conception to delivery; DCS/SCADA/MES/Historian
Excellent contract rates
Long term contract
Karen McHugh is the consultant managing this position.
If you are a CSV Engineer interested in roles based in Dublin, you can contact Karen by e-mail at firstname.lastname@example.org or phone +353-1-7978720 for a confidential chat.
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