Process Engineer

Overview Working with a Customer in the greater Cork area, we are looking for an experienced Process Engineer to join out Client Team to support the start-up of a new Process Manufacturing Suite. The position will be full time on site - a 12 month contracting position. Responsibilities Your day to day activities will include the following, however, every day is different and other items will come in your direction for completion. Strategic technical support of facility expansion for a new manufacturing suite onsite – Review and qualification of PFDs, P&IDs and sizing calculations. Technical process support of Vaccine Manufacture. Liaising with Site Management, commercialisation and cross functional teams to carry out investigations, deviations and to deliver process optimisation. Will address technical queries within the manufacturing process. Prepare, review and present technical documentation and findings pertaining to process performance - e.g. Qualifications and results of investigations. Coordination with design, site management and maintenance teams with regard to maintenance and reliability of process equipment. Ownership of equipment modules and process packages throughout start up. Completion of Risk Assessments. Participation in Technical and Safety reviews. Process optimization/site support. Qualifications You will have a degree in Chemical/Process Engineering (or equivalent) and will also have 3+ years of experience in the Pharmaceutical and Biopharmaceutical sector.Your day to day activities will include the following, however, every day is different and other items will come in your direction for completion. Strategic technical support of facility expansion for a new manufacturing suite onsite – Review and qualification of PFDs, P&IDs and sizing calculations. Technical process support of Vaccine Manufacture. Liaising with Site Management, commercialisation and cross functional teams to carry out investigations, deviations and to deliver process optimisation. Will address technical queries within the manufacturing process. Prepare, review and present technical documentation and findings pertaining to process performance - e.g. Qualifications and results of investigations. Coordination with design, site management and maintenance teams with regard to maintenance and reliability of process equipment. Ownership of equipment modules and process packages throughout start up. Completion of Risk Assessments. Participation in Technical and Safety reviews. Process optimization/site support.You will have a degree in Chemical/Process Engineering (or equivalent) and will also have 3+ years of experience in the Pharmaceutical and Biopharmaceutical sector.