Summary: Our client is a global Biopharmaceutical company based in Athlone is currently looking for a Manufacturing Process Engineer who will be responsible for delivering production related GMP projects within its Fill Finish facility.
Responsibilities: Assisting team members as directed for existing Aseptic Filling Lines.
Involvement/leading process improvement projects as directed.
Practical problem solving and root case analysis.
Process parameter monitoring and control, yield analysis.
Follow through on actions logs, project milestones and presentations.
Look for new innovative technologies.
Build a deep understanding of process variables.
Daily, weekly & monthly reporting of product and process metrics.
Work with quality management systems, process change management, ISO, FMEA, riskassessment, standard work documents.
Qualifications & Experience: Relevant engineering degree, NFQ Level 8 or higher.
Ideally Chemical, Mechanical, Manufacturing or Materials.
Knowledge of Six Sigma and lean systems is an advantage IT literacy will ideally include SQL databases and Minitab.
Experience in pharmaceutical processes is an advantage, particularly with Aseptic Processing(Partswasher, Autoclaves) & Filling (RABs or Isolator technologies).
Ability to examine data to grasp issues, draw conclusions, and solve problems.
Ability to make informed and timely decisions that take into account the facts, goals, constraints,and risks associated.
A team player with a can do, pro-active attitude and a passion for improvement.