Jr/Mid Level Process Engineer - Ireland - 12 Months ContractDo you want to be involved with exciting pharmaceutical projects?When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Jr/Mid Level Process Engineer.This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.*Essential Duties and Responsibilities for this role include, but are not limited to, the following:*Design/Author/Review/Approve/Execute qualification/validation documentation and process development studies in line with the standard approval processDesign/Author/Review/Approve/Execute Execution/development of change controlsTechnical input into quality notification by authoring/reviewing/approving investigationsExecution of equipment/qualification validation programs; including re-qualification and re-validationSupport continuous improvement through Lean Six Sigma methodologiesPerform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issuesServe as technical engineering representative for internal technical group discussions and represent technical Operations at global technical forumsDrive compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, ensuring consideration of the impact on GMP and compliance and decisions made.Desirable Experience:Demonstrable experience of leading technical related projectsPrevious experience with Automated visual inspection systems is desired, but not essential.Evidence of continuous professional development is desirableKnowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable but not a necessityKnowledge of regulatory/code requirements to Irish, European and International Codes, Standards and PracticesReport, standards, policy writing skills requiredEquipment and process validationIf this role is of interest to you, please apply now