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Our client has been providing Consulting Services to some of the worlds largest Pharmaceutical and Biotech Companies for over 10 years both in Ireland and abroad.

Due to further expansion they are looking for a Quality Systems Validation Engineer to join our team.

The ideal candidate will;
• Assess process Capabilities for discrete, well-defined processes
• Write clean and concise work instructions that can be understood by product builders
• Author technical reports, validations, and qualifications by capturing experimental results
• Author and complete proper documentation to meet quality systems requirements
• Writes validation protocols and reports applicable to new processes, including IQ,OQ and PQ.
• Gather and provide technical data for technical reviews
• Oversee qualification of builds associated with the project within the scope of the quality system
• Author/assist in the development of risk assessment for process, and develop URS and FDS for same

Competitive salaries, comprehensive benefits, a good working environment and a top class structure for career development all combine to make this company an attractive and exciting place to work for ambitious professionals.

To apply contact Catherine on 091- 563 868 or email cduggan@sigmar.ie